FDA 510(k) Applications Submitted by DAVID A OLSON

FDA 510(k) Number Submission Date Device Name Applicant
K032438 08/07/2003 MODIFICATION TO: MONOJET PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE, MONOJET PREFILL HEPRIN LOCK FLUSH SYRINGE TYCO HEALTHCARE
K033373 10/22/2003 MONOJECT INSULIN SYRINGE TYCO HEALTHCARE
K970266 01/23/1997 KENDALL HYDROPHILIC POWDER WOUND DRESSING KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K990530 02/19/1999 KERLIX MD ANTIMICROBIAL GAUZE DRESSING THE KENDALL COMPANY, L.P.
K970969 03/17/1997 KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET THE KENDAL CO.
K011283 04/27/2001 MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE THE KENDALL COMPANY
K961977 05/20/1996 KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K012736 08/16/2001 MONOJECT SAFETY NEEDLE TYCO HEALTHCARE
K963446 09/03/1996 KENDALL DUAL LUMEN CATHETER KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K973507 09/16/1997 KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317) KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K973511 09/17/1997 KENDALL CURITY PETROLATUM GAUZE KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K973619 09/23/1997 KENDALL CURITY NON-ADHERING DRESSING KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K973763 10/02/1997 KENDALL CURITY IODOFORM PACKING STRIP KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K954706 10/12/1995 KENDALL BLUNT TUOHY EPIDURAL NEEDLE KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K013556 10/25/2001 MONOJECT PREFILL HEPARIN LOCK FLUSH SYRINGE TYCO HEALTHCARE
K964519 11/12/1996 CURITY THORACENTESIS TRAY KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K964899 12/03/1996 KENDALL CURITY URETERAL CATHETER KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
K024010 12/04/2002 DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETER THE KENDALL COMPANY DIV. OF TYCO HEALTHCARE GROUP


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