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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