FDA 510(k) Applications Submitted by KATIE FORDYCE

FDA 510(k) Number Submission Date Device Name Applicant
K040038 01/08/2004 CURVED CUTTER STAPLER, MODELS CS40B, CS40G; RELOAD FOR CURVED STAPLER, MODELS CR40B, CR40G ETHICON ENDO-SURGERY, INC.
K030571 02/24/2003 ACUVANCE PLUS SAFETY IV CATHETER, PROTECTIV PLUS SAFETY IV CATHETER, OPTIVA IV CATHETER ETHICON ENDO-SURGERY, INC.
K011257 04/24/2001 ENDOPATH NON-BLADED OBTURATOR TROCAR SYSTEM (5 MM) ETHICON ENDO-SURGERY, INC.
K012128 07/09/2001 PROTECTIV ACUVANCE IV CATHETER SYSTEM ETHICON ENDO-SURGERY, INC.


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