Protek Medical Products, Inc.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Protek Medical Products, Inc.” (first 1997, latest 1998), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 98 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 |
|---|---|---|---|
| ITX | Transducer, Ultrasonic, Diagnostic | 5 | 5 |
| KKX | Drape, Surgical, Antimicrobial | 2 | 2 |
| FYA | Gown, Surgical | 1 | 1 |
| MMP | Cover, Barrier, Protective | 1 | 1 |
Review panels
- Radiology (5)
- General Hospital (4)
Most recent Protek Medical Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K973958 | GENERAL PURPOSE ATL NEEDLE GUIDE KIT | ITX | 1998-01-22 | 98 |
| K973622 | TRANSDUCER POSITIONER | ITX | 1997-11-26 | 64 |
| K970893 | ULTRASOUND TRANSDUCER DRAPE | FYA | 1997-10-20 | 223 |
| K970889 | ULTRASOUND TRANSDUCER DRAPE | KKX | 1997-10-20 | 223 |
| K973362 | NEEDLE GUIDE/GRID | ITX | 1997-10-01 | 23 |
| K970885 | ULTRASOUND SYSTEMS DRAPE | MMP | 1997-09-22 | 195 |
| K970891 | DRAPE, SURGICAL-LATEX | KKX | 1997-08-22 | 164 |
| K971722 | TRANS VAGINAL NEEDLE GUIDE | ITX | 1997-07-10 | 62 |
| K971115 | GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE | ITX | 1997-06-13 | 78 |
Recalls
openFDA lists no recalls under a recalling firm named Protek Medical 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.
- Protek, Inc. (25 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Protek Medical Products, Inc.?
FDA lists 9 510(k) clearances under the applicant name “Protek Medical Products, Inc.” (first 1997, latest 1998), 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 Protek Medical Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Protek Medical Products, Inc. is 98 days.
Which FDA product codes appear under Protek Medical Products, Inc.?
The most frequent FDA product codes under this applicant name are ITX (Transducer, Ultrasonic, Diagnostic, 5); KKX (Drape, Surgical, Antimicrobial, 2); FYA (Gown, Surgical, 1).
Next steps
- See all 9 Protek Medical Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code ITX, Protek Medical 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.