Janin Group, Inc.
FDA Regulatory Profile
Janin Group, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 4, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K012502 | MEDIGROUP CATHETER EXTENDER/REPAIR KIT | February 4, 2002 |
| K013017 | MEDIGROUP KEY TUBE | December 6, 2001 |
| K991042 | ASH ADVANTAGE PERITONEAL CATHETER | June 25, 1999 |
| K970159 | FLEX-NECK PD CATHETER | September 5, 1997 |
| K810512 | MEDISEAL CAMERA COVERS | March 13, 1981 |