Tyco Healthcare is one of 25971 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tyco Healthcare - FDA 510(k) Cleared Devices
Recent clearances: DOVER 100% SILICONE FOLEY CATHETER WITH TEMPERATURE SENSOR, KENDALL ANTIMICROBIAL DRAIN DRESSING FOR OTC USE, MODEL 6662, KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662
14
Total
14
Cleared
0
Denied
Tyco Healthcare has 14 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 14 cleared submissions from 2001 to 2007.
Browse the FDA 510(k) cleared devices submitted by Tyco Healthcare Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tyco Healthcare
14 devices
Cleared
Oct 16, 2007
DOVER 100% SILICONE FOLEY CATHETER WITH TEMPERATURE SENSOR
Gastroenterology & Urology
186d
Cleared
Sep 14, 2007
KENDALL ANTIMICROBIAL DRAIN DRESSING FOR OTC USE, MODEL 6662
General & Plastic Surgery
186d
Cleared
Sep 12, 2007
KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662
General & Plastic Surgery
187d
Cleared
Aug 03, 2006
MONOJECT MAGELLAN INSULIN AND TUBERCULIN SAFETY SYRINGE
General Hospital
64d
Cleared
Jan 18, 2005
DOVER SILVER TEMPERATURE SENSING FOLEY CATHETER
Gastroenterology & Urology
110d
Cleared
Jul 20, 2004
DOVER ROB-NEL CATHETER
Gastroenterology & Urology
105d
Cleared
Jul 15, 2004
KENDALL SCD EXPRESS KAMBIA THIGH LENGTH TEARAWAY SLEEVE
Cardiovascular
126d
Cleared
Jul 07, 2004
DOVER RED RUBBER ROBINSON CATHETER
Gastroenterology & Urology
57d
Cleared
Jun 30, 2004
MODIFICATION TO: MONOJET PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE, MONOJET...
General Hospital
328d
Cleared
Apr 29, 2004
KENDALL ULTEC PRO AG+ HYDROCOLLOID DRESSING
General & Plastic Surgery
182d
Cleared
Dec 08, 2003
KENDALL LIFETRACE UMBILICAL BLOOD COLLECTION KIT, CODE 56501
Hematology
89d
Cleared
Nov 13, 2003
MONOJECT INSULIN SYRINGE
General Hospital
22d