Clinical Convenience Products, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Clinical Convenience Products, Inc.” (first 1979, latest 1994), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 26 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 |
|---|---|---|---|
| JXA | Kit, Screening, Urine | 4 | 4 |
| JSI | Culture Media, Selective And Differential | 2 | 2 |
Review panels
- Microbiology (6)
Most recent Clinical Convenience Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K934759 | CULTURIA MACCONKEY-MUG | JXA | 1994-09-09 | 340 |
| K870502 | CULTURIA MACCONKEY-MUG/MODIFIED TSA SYSTEMS | JSI | 1987-02-26 | 22 |
| K864764 | CULTURIA MACCONKEY-MUG/CLED SYSTEMS | JSI | 1986-12-29 | 24 |
| K800215 | CULTURIA MACCONKEY/CLED #DM87 | JXA | 1980-02-13 | 9 |
| K792579 | CULTURIA MACCONKEY/COLUMBIA CNA | JXA | 1980-01-11 | 28 |
| K792284 | CULTURIA EMB/COLUMBIA CNA W/5% SHEEP | JXA | 1979-12-19 | 36 |
Recalls
openFDA lists no recalls under a recalling firm named Clinical Convenience 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.
- Clinical Data, Inc. (37 510(k)s)
- Clinical Sciences, Inc. (30 510(k)s)
- Clinical Assays, Inc. (27 510(k)s)
- Clinical Controls, Inc. (18 510(k)s)
- Clinical Innovations, LLC (18 510(k)s)
- Clinical Resources, Inc. (14 510(k)s)
- Clinical Technology Corp. (12 510(k)s)
- Clinical Connections, Inc. (10 510(k)s)
- Clinical Diagnostics, Inc. (8 510(k)s)
- Clinical Laserthermia Systems, AB (6 510(k)s)
- Clinical Neuro Systems, LLC (5 510(k)s)
- Clinical Bioresearch (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Clinical Convenience Products, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Clinical Convenience Products, Inc.” (first 1979, latest 1994), across 2 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 Clinical Convenience Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Clinical Convenience Products, Inc. is 26 days.
Which FDA product codes appear under Clinical Convenience Products, Inc.?
The most frequent FDA product codes under this applicant name are JXA (Kit, Screening, Urine, 4); JSI (Culture Media, Selective And Differential, 2).
Next steps
- See all 6 Clinical Convenience Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JXA, Clinical Convenience 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.