Thompson Respiration Products, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Thompson Respiration Products, Inc.” (first 1978, latest 1982), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 160 days. 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 |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| CBK | Ventilator, Continuous, Facility Use | 4 | 4 |
| BZQ | Monitor, Breathing Frequency | 1 | 1 |
| CAP | Monitor, Airway Pressure (Includes Gauge And/Or Alarm) | 1 | 1 |
Review panels
- Anesthesiology (6)
Most recent Thompson Respiration Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K822103 | MODEL M3000XA VENTILATOR SPECIFICA | CBK | 1982-07-26 | 10 |
| K782174 | PRESSURE ALARM | CAP | 1979-01-22 | 34 |
| K781158 | ALARM UNIT, BATTERY OPERATED | BZQ | 1978-12-18 | 166 |
| K781160 | VENTILATOR, MINILUNG | CBK | 1978-12-13 | 161 |
| K781159 | VENTILATOR, PRESSURE | CBK | 1978-12-12 | 160 |
| K781161 | RESPIRATOR, BANTAM MODEL | CBK | 1978-12-11 | 159 |
Recalls
openFDA lists no recalls under a recalling firm named Thompson Respiration Products, Inc..
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.
- Thompson Surgical Instruments, Inc. (3 510(k)s)
- Thompson Mis, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Thompson Respiration Products, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Thompson Respiration Products, Inc.” (first 1978, latest 1982), across 3 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Thompson Respiration Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Thompson Respiration Products, Inc. is 160 days.
Which FDA product codes appear under Thompson Respiration Products, Inc.?
The most frequent FDA product codes under this applicant name are CBK (Ventilator, Continuous, Facility Use, 4); BZQ (Monitor, Breathing Frequency, 1); CAP (Monitor, Airway Pressure (Includes Gauge And/Or Alarm), 1).
Next steps
- See all 6 Thompson Respiration Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code CBK, Thompson Respiration Products, Inc.'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.