Preferred Medical Products: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Preferred Medical Products” (first 1989, latest 1995), across 3 product codes in 3 review panels. Median 510(k) review time under this name: 238 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 |
|---|---|---|---|
| CAZ | Anesthesia Conduction Kit | 4 | 4 |
| IPF | Stimulator, Muscle, Powered | 1 | 1 |
| KKX | Drape, Surgical, Antimicrobial | 1 | 1 |
Review panels
- Anesthesiology (4)
- General Hospital (1)
- Physical Medicine (1)
Most recent Preferred Medical Products 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K941153 | EPI-SPINAL ANESTHESIA TRAY | CAZ | 1995-05-30 | 445 |
| K924699 | PMP MUSCLE STIMULATOR | IPF | 1993-04-30 | 225 |
| K920808 | OB/GYN DRAPE | KKX | 1993-02-19 | 364 |
| K904440 | LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS | CAZ | 1991-06-07 | 252 |
| K885278 | EPIDURAL ANESTHESIA TRAY | CAZ | 1989-03-16 | 83 |
| K885277 | SPINAL ANESTHESIA TRAY | CAZ | 1989-03-06 | 73 |
Recalls
openFDA lists no recalls under a recalling firm named Preferred Medical Products.
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.
- Preferred Micro-Media (28 510(k)s)
- Preferred Instruments (1 510(k)s)
- Preferred Medical Devices, Inc. (1 510(k)s)
- Preferred Medical Supply, Inc. (1 510(k)s)
- Preferred Optics, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Preferred Medical Products?
FDA lists 6 510(k) clearances under the applicant name “Preferred Medical Products” (first 1989, latest 1995), across 3 product codes in 3 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 Preferred Medical Products?
The median time from FDA receipt to decision across 510(k)s cleared under the name Preferred Medical Products is 238 days.
Which FDA product codes appear under Preferred Medical Products?
The most frequent FDA product codes under this applicant name are CAZ (Anesthesia Conduction Kit, 4); IPF (Stimulator, Muscle, Powered, 1); KKX (Drape, Surgical, Antimicrobial, 1).
Next steps
- See all 6 Preferred Medical Products clearances with predicates and recalls
- Run predicate analysis for product code CAZ, Preferred Medical Products'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.