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FDA 510(k) Applications Submitted by PAUL W EVANS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K002901
09/18/2000
KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER
THE KENDALL COMPANY
K990500
02/17/1999
KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C
THE KENDAL CO.
K070653
03/09/2007
KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662
TYCO HEALTHCARE
K070685
03/12/2007
KENDALL ANTIMICROBIAL DRAIN DRESSING FOR OTC USE, MODEL 6662
TYCO HEALTHCARE
K992079
06/21/1999
KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325
THE KENDALL COMPANY, L.P.
K061936
07/10/2006
KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311
THE KENDALL COMPANY
K042461
09/10/2004
KENDALL ARGYLE 2 FR DOUBLE LUMEN NEONATAL/PEDIATRIC PICC, MODEL 43304
KENDALL
K973546
09/18/1997
KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
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