Tyco Healthcare Group LP is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tyco Healthcare Group LP - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Tyco Healthcare Group LP has 4 FDA 510(k) cleared medical devices. Based in Norwalk, US.
Historical record: 4 cleared submissions from 2001 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tyco Healthcare Group LP Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tyco Healthcare Group LP
4 devices
Cleared
May 05, 2008
AUTO SUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS WITH...
General & Plastic Surgery
35d
Cleared
Nov 19, 2007
COPA AMD ANTIMICROBIAL WOUND DRESSING
General & Plastic Surgery
187d
Cleared
May 22, 2006
GENIUS 2 INFRARED TYMPANIC ELECTRONIC THERMOMETER, MODEL 303000
General Hospital
70d
Cleared
Apr 09, 2001
NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE
General & Plastic Surgery
14d