Alamar: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Alamar” (first 1991, latest 1991), across 1 product code in 1 review panel. Median 510(k) review time under this name: 40 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 |
|---|---|---|---|
| JWY | Manual Antimicrobial Susceptibility Test Systems | 7 | 7 |
Review panels
- Microbiology (7)
Most recent Alamar 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K911392 | ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (CEFOTETAN | JWY | 1991-05-08 | 40 |
| K911391 | ANTIMICROBIAL SUSCEPT. TEST PANEL (CEFTIZOXIME) | JWY | 1991-05-08 | 40 |
| K911390 | ANTIMICROBIAL SUSCEPT. TEST PANEL(TRIMETHOPRIM) | JWY | 1991-05-08 | 40 |
| K911389 | ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL (IMIPENEM) | JWY | 1991-05-08 | 40 |
| K910484 | ANTIMICROBIAL SUSCEPTIBILITY TEST PANEL | JWY | 1991-03-11 | 33 |
| K910346 | ANTIMICROBIAL CEFTRIAXONE | JWY | 1991-02-25 | 28 |
| K910345 | ANTIMICROBIAL CEFOPERAZONE | JWY | 1991-02-25 | 28 |
Recalls
openFDA lists no recalls under a recalling firm named Alamar.
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.
- Alamar Biosciences Laboratory, Inc. (26 510(k)s)
- Alamar Biosciences, Inc. (5 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Alamar?
FDA lists 7 510(k) clearances under the applicant name “Alamar” (first 1991, latest 1991), across 1 product code 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 Alamar?
The median time from FDA receipt to decision across 510(k)s cleared under the name Alamar is 40 days.
Which FDA product codes appear under Alamar?
The most frequent FDA product codes under this applicant name are JWY (Manual Antimicrobial Susceptibility Test Systems, 7).
Next steps
- See all 7 Alamar clearances with predicates and recalls
- Run predicate analysis for product code JWY, Alamar'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.