Company ยท US
Breit Laboratories, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1985. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 25, 1985 | K851099 | IGM RHEUMATOID FACTOR TEST KIT Breit Laboratories, Inc. | DHR |
| Sep 5, 1984 | K842137 | OCCULT BLOOD TEST Breit Laboratories, Inc. | KHE |
| Sep 5, 1984 | K840527 | COLOTRAK OCCULT BLOOD TEST Breit Laboratories, Inc. | KHE |
| Aug 11, 1983 | K832031 | ANTI-N DNA ANTIBODY TEST KIT Breit Laboratories, Inc. | KTL |
| Jul 18, 1983 | K831927 | ANTINUCLEAR ANTIBODY TEST KIT Breit Laboratories, Inc. | DAA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||