Clayton Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K833860 | TUCK-TITE COLON FLUID RETAINER | December 27, 1983 |
| K790535 | CLAYTON COLON CLEANSING KIT | June 7, 1979 |