Company ยท US
Janin Group, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 2002. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 4, 2002 | K012502 | MEDIGROUP CATHETER EXTENDER/REPAIR KIT Janin Group, Inc. | FJS |
| Dec 6, 2001 | K013017 | MEDIGROUP KEY TUBE Janin Group, Inc. | FJS |
| Jun 25, 1999 | K991042 | ASH ADVANTAGE PERITONEAL CATHETER Janin Group, Inc. | FJS |
| Sep 5, 1997 | K970159 | FLEX-NECK PD CATHETER Janin Group, Inc. | FJS |
| Mar 13, 1981 | K810512 | MEDISEAL CAMERA COVERS Janin Group, Inc. | KQM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||