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Neurodynamics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K932402
MODIFICATION TO GHAJAR GUIDE TWIST DRILL
August 5, 1993
K875205
TRI-FLOW CATHETER
May 31, 1988
K875018
GHAJAR GUIDE TWIST DRILL
January 28, 1988
K875019
GHAJAR GUIDE SYSTEM FOR THE PERFORATOR
January 22, 1988