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Gerard Medical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K974533
TRIMPORT
May 7, 1998
K972555
CATHETER TUNNELER
December 22, 1997
K945060
HERNIA MESH INTRODUCTION SYSTEM
March 2, 1995
K936207
ENDO-NEEDLE INSTRUMENT
June 16, 1994