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FDA 510(k) Applications Submitted by LISA CRISSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010779
03/15/2001
MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT
GIBBONS SURGICAL CORP.
K012198
07/13/2001
GIBBONS STERILE TROCAR KITS
GIBBONS SURGICAL CORP.
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