Lafayette Pharmacal, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K931896 | PRO-FLO SYSTEM | August 26, 1993 |
| K884379 | MAGLINTE ENTEROCLYSIS CATHETER | February 28, 1989 |
| K881609 | SITZMARKS | July 8, 1988 |
| K860441 | ENTROKIT WITH MAGLINTE CATHETER | March 12, 1986 |