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Gibbons Surgical Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K012198
GIBBONS STERILE TROCAR KITS
August 9, 2001
K010779
MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT
April 10, 2001