Breit Laboratories, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Breit Laboratories, Inc.” (first 1983, latest 1985), across 4 product codes in 3 review panels. Median 510(k) review time under this name: 49 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 |
|---|---|---|---|
| KHE | Reagent, Occult Blood | 2 | 2 |
| DAA | Igg, Peroxidase, Antigen, Antiserum, Control | 1 | 1 |
| DHR | System, Test, Rheumatoid Factor | 1 | 1 |
| KTL | Anti-Dna Indirect Immunofluorescent Solid Phase | 1 | 1 |
Review panels
- Hematology (2)
- Immunology (2)
- Pathology (1)
Most recent Breit Laboratories, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K851099 | IGM RHEUMATOID FACTOR TEST KIT | DHR | 1985-04-25 | 37 |
| K842137 | OCCULT BLOOD TEST | KHE | 1984-09-05 | 98 |
| K840527 | COLOTRAK OCCULT BLOOD TEST | KHE | 1984-09-05 | 211 |
| K832031 | ANTI-N DNA ANTIBODY TEST KIT | KTL | 1983-08-11 | 49 |
| K831927 | ANTINUCLEAR ANTIBODY TEST KIT | DAA | 1983-07-18 | 33 |
Recalls
openFDA lists no recalls under a recalling firm named Breit Laboratories, 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Breit Laboratories, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Breit Laboratories, Inc.” (first 1983, latest 1985), across 4 product codes in 3 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Breit Laboratories, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Breit Laboratories, Inc. is 49 days.
Which FDA product codes appear under Breit Laboratories, Inc.?
The most frequent FDA product codes under this applicant name are KHE (Reagent, Occult Blood, 2); DAA (Igg, Peroxidase, Antigen, Antiserum, Control, 1); DHR (System, Test, Rheumatoid Factor, 1).
Next steps
- See all 5 Breit Laboratories, Inc. clearances with predicates and recalls
- Run predicate analysis for product code KHE, Breit Laboratories, 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.