Squibb & Sons, Inc.
FDA Regulatory Profile
Squibb & Sons, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 14, 1982.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K821174 | TSH-SQUIBB RADIOIMMUNOASSAY KIT | May 14, 1982 |
| K801424 | ESTRIOL RIA KIT FOR USE WITH GAMMAFLO | July 21, 1980 |
| K800750 | STOMAHESIVE STERILE WAFER | May 8, 1980 |
| K770726 | RIA KIT, T4 CLASP | April 28, 1977 |
| K761267 | ANGIOTENSIN I IMMUTOPE KIT | December 30, 1976 |