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Janin Group, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K012502MEDIGROUP CATHETER EXTENDER/REPAIR KITFebruary 4, 2002
K013017MEDIGROUP KEY TUBEDecember 6, 2001
K991042ASH ADVANTAGE PERITONEAL CATHETERJune 25, 1999
K970159FLEX-NECK PD CATHETERSeptember 5, 1997
K810512MEDISEAL CAMERA COVERSMarch 13, 1981