Cappel Diagnostics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K872839 | ANTINUCLEAR ANTIBODY TEST | October 20, 1987 |
| K864275 | ANTI-NDNA ANTIBODY TEST KIT | December 15, 1986 |
| K862821 | CAPPEL DIAGNOSTICS ANA KIT | August 15, 1986 |