Tyco Healthcare is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tyco Healthcare - FDA 510(k) Cleared Devices
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
Cleared
Dec 31, 2001
MONOJECT PREFILL HEPARIN LOCK FLUSH SYRINGE
General Hospital
67d
Cleared
Oct 25, 2001
MONOJECT SAFETY NEEDLE
General Hospital
70d