Preferred Micro-Media: FDA filings under this applicant name
FDA lists 28 510(k) clearances under the applicant name “Preferred Micro-Media” (first 1985, latest 1985), across 7 product codes in 1 review panel. Median 510(k) review time under this name: 22 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 |
|---|---|---|---|
| JSI | Culture Media, Selective And Differential | 9 | 9 |
| JSJ | Culture Media, Selective And Non-Differential | 7 | 7 |
| JSH | Culture Media, Non-Selective And Differential | 5 | 5 |
| JSG | Culture Media, Non-Selective And Non-Differential | 2 | 2 |
| JTY | Culture Media, For Isolation Of Pathogenic Neisseria | 2 | 2 |
| KZI | Culture Media, Enriched | 2 | 2 |
| JTZ | Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth | 1 | 1 |
Review panels
- Microbiology (28)
Most recent Preferred Micro-Media 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K851594 | SF BROTH | JSI | 1985-05-14 | 28 |
| K851597 | TRIPLE SUGAR IRON AGAR | JSH | 1985-05-13 | 27 |
| K851596 | SIM MEDIUM | JSH | 1985-05-13 | 27 |
| K851595 | SIMMONS CITRATE AGAR | JSH | 1985-05-13 | 27 |
| K851593 | SELECTIVE STREPTOCOCCUS AGAR | JSJ | 1985-05-13 | 27 |
| K851592 | SABOURAUD DEXTROSE AGAR | JSJ | 1985-05-13 | 27 |
| K851591 | PHENYLETHYL ALCOHOL AGAR W/5%SHEEP BLOOD | JSJ | 1985-05-13 | 27 |
| K851598 | THIOGLYCOLLATE WITHOUT INDICATOR | JSG | 1985-05-10 | 24 |
| K851576 | BIGGY AGAR NICKERSONS MEDIUM | JSH | 1985-05-09 | 23 |
| K851603 | XYLOSE LYSINE DESOXYCHOLATE AGAR | JSI | 1985-05-08 | 22 |
18 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Preferred Micro-Media.
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 Medical Products (6 510(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 Micro-Media?
FDA lists 28 510(k) clearances under the applicant name “Preferred Micro-Media” (first 1985, latest 1985), across 7 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 Preferred Micro-Media?
The median time from FDA receipt to decision across 510(k)s cleared under the name Preferred Micro-Media is 22 days.
Which FDA product codes appear under Preferred Micro-Media?
The most frequent FDA product codes under this applicant name are JSI (Culture Media, Selective And Differential, 9); JSJ (Culture Media, Selective And Non-Differential, 7); JSH (Culture Media, Non-Selective And Differential, 5).
Next steps
- See all 28 Preferred Micro-Media clearances with predicates and recalls
- Run predicate analysis for product code JSI, Preferred Micro-Media'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.