Board of Directors, Albert Browne , Ltd.: FDA clearances and approvals
Board of Directors, Albert Browne , Ltd. has 5 FDA 510(k) clearances (first 1990, latest 1998), across 1 product code in 1 review panel. Median 510(k) review time: 407 days.
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 |
|---|---|---|---|
| JOJ | Indicator, Physical/Chemical Sterilization Process | 5 | 5 |
Review panels
- General Hospital (5)
Most recent Board of Directors, Albert Browne , Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K971971 | BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACK | JOJ | 1998-07-10 | 407 |
| K970918 | BROWNE STEAM INDICATOR | JOJ | 1997-06-24 | 104 |
| K932057 | BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK | JOJ | 1994-08-05 | 464 |
| K922481 | BROWNE GA INDICATOR USE IN 2% ACTIV GLUTARALDEHYDE | JOJ | 1994-06-02 | 737 |
| K902958 | TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE | JOJ | 1990-11-01 | 119 |
Recalls
openFDA lists no recalls under a recalling firm named Board of Directors, Albert Browne , Ltd..
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Board of Directors, Albert Browne , Ltd. have?
Board of Directors, Albert Browne , Ltd. has 5 FDA 510(k) clearances (first 1990, latest 1998), across 1 product code in 1 review panel.
How long does FDA take to clear Board of Directors, Albert Browne , Ltd.'s 510(k)s?
The median time from FDA receipt to decision across Board of Directors, Albert Browne , Ltd.'s cleared 510(k)s is 407 days.
What devices does Board of Directors, Albert Browne , Ltd. make?
Its most frequent FDA product codes are JOJ (Indicator, Physical/Chemical Sterilization Process, 5).
Has Board of Directors, Albert Browne , Ltd. had device recalls?
openFDA lists no recalls under a recalling firm name matching Board of Directors, Albert Browne , Ltd. Related entities may recall under other names.
Next steps
- See all 5 Board of Directors, Albert Browne , Ltd. clearances with predicates and recalls
- Run predicate analysis for product code JOJ, Board of Directors, Albert Browne , Ltd.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.