Immuno-Diagnostic Laboratories
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K833777 | ANGIOTENSIN CONVERTING ENZYME | January 30, 1984 |
| K811394 | CEA DESALTING DOLUMN SEPHADEX R | June 12, 1981 |