Janin Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Janin Group, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Janin Group, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1981 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Janin Group, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Janin Group, Inc.
5 devices
Cleared
Feb 04, 2002
MEDIGROUP CATHETER EXTENDER/REPAIR KIT
Gastroenterology & Urology
185d
Cleared
Dec 06, 2001
MEDIGROUP KEY TUBE
Gastroenterology & Urology
90d
Cleared
Jun 25, 1999
ASH ADVANTAGE PERITONEAL CATHETER
Gastroenterology & Urology
88d
Cleared
Sep 05, 1997
FLEX-NECK PD CATHETER
Gastroenterology & Urology
232d
Cleared
Mar 13, 1981
MEDISEAL CAMERA COVERS
General & Plastic Surgery
17d