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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