Gerard Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K974533TRIMPORTMay 7, 1998
K972555CATHETER TUNNELERDecember 22, 1997
K945060HERNIA MESH INTRODUCTION SYSTEMMarch 2, 1995
K936207ENDO-NEEDLE INSTRUMENTJune 16, 1994