Central Media: FDA filings under this applicant name
FDA lists 14 510(k) clearances under the applicant name “Central Media” (first 1987, latest 1987), across 5 product codes in 1 review panel. Median 510(k) review time under this name: 85 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 | 8 | 8 |
| JSH | Culture Media, Non-Selective And Differential | 2 | 2 |
| KZI | Culture Media, Enriched | 2 | 2 |
| JSG | Culture Media, Non-Selective And Non-Differential | 1 | 1 |
| JTZ | Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth | 1 | 1 |
Review panels
- Microbiology (14)
Most recent Central Media 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K873260 | CORYNEBACTERIA ISOLATION MEDIA | JSI | 1987-11-06 | 87 |
| K873259 | SPECIALTY MEDIA | JSI | 1987-11-06 | 87 |
| K873258 | STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIA | JSI | 1987-11-06 | 87 |
| K873257 | GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA. | JSG | 1987-11-06 | 87 |
| K873270 | ACTINOMYCETE DIFFERENTIAL MEDIA | JSH | 1987-11-04 | 85 |
| K873269 | MYCOLOGICAL MEDIA | JSI | 1987-11-04 | 85 |
| K873268 | MUELLER HINTON MEDIA | JTZ | 1987-11-04 | 85 |
| K873267 | ECG BASED MEDIA | KZI | 1987-11-04 | 85 |
| K873266 | MIDDLEBROOK BASED MEDIA | KZI | 1987-10-28 | 78 |
| K873265 | MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION | JSI | 1987-10-28 | 78 |
4 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Central 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.
- Central Medicare Sdn Bhd (15 510(k)s)
- Central Solutions, Inc. (7 510(k)s)
- Central Biological Co. (5 510(k)s)
- Central Georgia Ancillary Health Systems (3 510(k)s)
- Central Labs. Assoc. MD Pathologists (3 510(k)s)
- Central Plastic, Inc. (2 510(k)s)
- Central Chemical Co., Ltd. (1 510(k)s)
- Central Equipment Sales, Inc. (1 510(k)s)
- Central Illinois Hearing Aid Centers, Inc. (1 510(k)s)
- Central Pharmaceuticals, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Central Media?
FDA lists 14 510(k) clearances under the applicant name “Central Media” (first 1987, latest 1987), across 5 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 Central Media?
The median time from FDA receipt to decision across 510(k)s cleared under the name Central Media is 85 days.
Which FDA product codes appear under Central Media?
The most frequent FDA product codes under this applicant name are JSI (Culture Media, Selective And Differential, 8); JSH (Culture Media, Non-Selective And Differential, 2); KZI (Culture Media, Enriched, 2).
Next steps
- See all 14 Central Media clearances with predicates and recalls
- Run predicate analysis for product code JSI, Central 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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.