Breit Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K851099 | IGM RHEUMATOID FACTOR TEST KIT | April 25, 1985 |
| K840527 | COLOTRAK OCCULT BLOOD TEST | September 5, 1984 |
| K842137 | OCCULT BLOOD TEST | September 5, 1984 |
| K832031 | ANTI-N DNA ANTIBODY TEST KIT | August 11, 1983 |
| K831927 | ANTINUCLEAR ANTIBODY TEST KIT | July 18, 1983 |