Automated Medical Products Corp.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Automated Medical Products Corp.” (first 1979, latest 1995), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 72 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 |
|---|---|---|---|
| GAD | Retractor | 2 | 2 |
| GCJ | Laparoscope, General & Plastic Surgery | 2 | 2 |
| LDD | Dc-Defibrillator, Low-Energy, (Including Paddles) | 1 | 1 |
| MDM | Instrument, Manual, Surgical, General Use | 1 | 1 |
Review panels
Most recent Automated Medical Products Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K942910 | DEEPVISON | GCJ | 1995-07-21 | 395 |
| K942818 | DEEP SUTURE | MDM | 1994-08-25 | 71 |
| K942002 | RETRACTOR | GAD | 1994-05-17 | 22 |
| K940199 | DISSECTOR | GCJ | 1994-03-30 | 76 |
| K832827 | CORPULS 300 | LDD | 1983-11-03 | 73 |
| K792145 | AUTOMATIC RETRACTOR HOLDERS | GAD | 1979-12-05 | 43 |
Recalls
openFDA lists no recalls under a recalling firm named Automated Medical Products Corp..
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.
- Automated Screening Devices (2 510(k)s)
- Automated IV Systems, Inc. (1 510(k)s)
- Automated Lens System (1 510(k)s)
- Automated Ophthalmics, Inc. (1 510(k)s)
- Automated Testing Services, Ltd. (1 510(k)s)
- Automated Imaging Diagnostics, LLC (0 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Automated Medical Products Corp.?
FDA lists 6 510(k) clearances under the applicant name “Automated Medical Products Corp.” (first 1979, latest 1995), across 4 product codes in 2 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 Automated Medical Products Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Automated Medical Products Corp. is 72 days.
Which FDA product codes appear under Automated Medical Products Corp.?
The most frequent FDA product codes under this applicant name are GAD (Retractor, 2); GCJ (Laparoscope, General & Plastic Surgery, 2); LDD (Dc-Defibrillator, Low-Energy, (Including Paddles), 1).
Next steps
- See all 6 Automated Medical Products Corp. clearances with predicates and recalls
- Run predicate analysis for product code GAD, Automated Medical Products Corp.'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.