Beijing Choice Electronic Technology Co., Ltd.: FDA filings under this applicant name
FDA lists 14 510(k) clearances under the applicant name “Beijing Choice Electronic Technology Co., Ltd.” (first 2016, latest 2024), across 5 product codes in 4 review panels. Median 510(k) review time under this name: 223 days. Since 2017 the median was 224 days, against 182 days for all cleared 510(k)s in the same product codes. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2016 | 3 | 222 |
| 2017 | 1 | 197 |
| 2018 | 2 | 175 |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 1 | 161 |
| 2022 | 3 | 228 |
| 2023 | 3 | 273 |
| 2024 | 1 | 274 |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Beijing Choice Electronic Technology Co., Ltd. took a median 224 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 182 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| DQA | Oximeter | 10 | 10 |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | 1 | 1 |
| FLL | Continuous Measurement Thermometer | 1 | 1 |
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | 1 | 1 |
| NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter | 1 | 1 |
Review panels
- Anesthesiology (10)
- Cardiovascular (2)
- General Hospital (1)
- Neurology (1)
Most recent Beijing Choice Electronic Technology Co., Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K232975 | Pulse Oximeter (MD300C228) | DQA | 2024-06-21 | 274 |
| K230587 | Wrist Pulse Oximeter | DQA | 2023-11-30 | 273 |
| K230172 | Pulse Oximeter | DQA | 2023-08-12 | 204 |
| K220101 | Pulse Oximeter | DQA | 2023-03-08 | 420 |
| K221992 | Electronic Pulse Stimulator | NUH | 2022-10-21 | 107 |
| K211400 | Pulse Oximeter | DQA | 2022-02-11 | 282 |
| K211752 | Infrared Thermometer | FLL | 2022-01-21 | 228 |
| K211754 | Vital Signs Monitor | MWI | 2021-11-15 | 161 |
| K181503 | Fingertip Pulse Oximeter | DQA | 2018-10-11 | 126 |
| K172366 | Wrist Pulse Oximeter | DQA | 2018-03-16 | 224 |
4 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Beijing Choice Electronic Technology Co., Ltd..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Beijing Choice Electronic Technololgy Co., Ltd. (29 510(k)s)
- Beijing Adss Development Co., Ltd. (10 510(k)s)
- Beijing Biosis Healing Biolog Ical Technology Co., Ltd. (7 510(k)s)
- Beijing East Whale Imaging Technology Co., Ltd. (6 510(k)s)
- Beijing Nubway S&T Co., Ltd. (6 510(k)s)
- Beijing Sano Laser S&T Development Co.,Ltd (6 510(k)s)
- Beijing Zksk Technology Co., Ltd. (6 510(k)s)
- Beijing Honkon Technologies Co., Ltd. (5 510(k)s)
- Beijing Superlaser Technology Co., Ltd. (5 510(k)s)
- Beijing Demax Medical Technology Co.,Ltd (4 510(k)s)
- Beijing Fule Science & Technology Development Co., Ltd. (4 510(k)s)
- Beijing Globalipl Development Co., Ltd. (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Beijing Choice Electronic Technology Co., Ltd.?
FDA lists 14 510(k) clearances under the applicant name “Beijing Choice Electronic Technology Co., Ltd.” (first 2016, latest 2024), across 5 product codes in 4 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Beijing Choice Electronic Technology Co., Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Beijing Choice Electronic Technology Co., Ltd. is 223 days. Since 2017: 224 days, versus 182 days for all cleared 510(k)s in the same product codes.
Which FDA product codes appear under Beijing Choice Electronic Technology Co., Ltd.?
The most frequent FDA product codes under this applicant name are DQA (Oximeter, 10); DXN (System, Measurement, Blood-Pressure, Non-Invasive, 1); FLL (Continuous Measurement Thermometer, 1).
Next steps
- See all 14 Beijing Choice Electronic Technology Co., Ltd. clearances with predicates and recalls
- Run predicate analysis for product code DQA, Beijing Choice Electronic Technology Co., Ltd.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.