Hancock Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K801885 | HANCOCK * OBTURATORS | September 9, 1980 |
| K800703 | MODIFIED CATHETER PACKAGE | April 8, 1980 |
| K800122 | HANCOCK AORTIC PUNCH | February 1, 1980 |
| K790534 | MERSILENE SUTURES | March 26, 1979 |
| K780568 | DURAN FLEXIBLE RING | May 26, 1978 |