The Kendall Company, L.P.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K990530 | KERLIX MD ANTIMICROBIAL GAUZE DRESSING | January 31, 2000 |
| K992079 | KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325 | September 29, 1999 |