Interstate Media: FDA filings under this applicant name
FDA lists 15 510(k) clearances under the applicant name “Interstate Media” (first 1982, latest 1982), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 20 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 | 4 | 4 |
| JTZ | Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth | 3 | 3 |
Review panels
- Microbiology (15)
Most recent Interstate Media 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K821431 | XLD AGAR | JSI | 1982-06-01 | 20 |
| K821430 | MUELLER HINTON MEDIUM | JTZ | 1982-06-01 | 20 |
| K821429 | MUELLER HINTON MED. W/5% SHEEP BLOOD | JTZ | 1982-06-01 | 20 |
| K821428 | MUELLER HINTON CHOCOLATE MED. ENRICHED | JTZ | 1982-06-01 | 20 |
| K821427 | MANNITOL SALT AGAR | JSI | 1982-06-01 | 20 |
| K821426 | STAPHYLOCOCCUS MEDIUM 1100 | JSI | 1982-06-01 | 20 |
| K821425 | COLUMBIA BLOOD AGAR W/5% SHEEP BLOOD | JSH | 1982-06-01 | 20 |
| K821424 | TRYPTIC SOY AGAR W/5% SHEEP BLOOD | JSH | 1982-06-01 | 20 |
| K821423 | MACCONKEY AGAR | JSI | 1982-06-01 | 20 |
| K821422 | SS AGAR | JSI | 1982-06-01 | 20 |
5 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Interstate 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.
- Interstate Dental Co., Inc. (2 510(k)s)
- Interstate Hearing Aid Service (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Interstate Media?
FDA lists 15 510(k) clearances under the applicant name “Interstate Media” (first 1982, latest 1982), across 3 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 Interstate Media?
The median time from FDA receipt to decision across 510(k)s cleared under the name Interstate Media is 20 days.
Which FDA product codes appear under Interstate 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, 4); JTZ (Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth, 3).
Next steps
- See all 15 Interstate Media clearances with predicates and recalls
- Run predicate analysis for product code JSI, Interstate 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.