Covidien Lp, Formerly Registered AS Tyco Healthcar is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covidien Lp, Formerly Registered AS Tyco Healthcar - FDA 510(k) Clear...
4
Total
4
Cleared
0
Denied
Covidien Lp, Formerly Registered AS Tyco Healthcar has 4 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 4 cleared submissions from 2007 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Covidien Lp, Formerly Registered AS Tyco Healthcar Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Covidien Lp, Formerly Registered AS Tyco Healthcar
4 devices
Cleared
Apr 26, 2010
VERSAPORT BLADELESS LOW PROFILE TROCAR MODEL NB3SHFLP, NB5SHFLP, NB5STFLP
General & Plastic Surgery
59d
Cleared
Dec 03, 2009
SILS PORT MODEL SILSPT15
General & Plastic Surgery
35d
Cleared
Feb 26, 2009
COPA AMD
General & Plastic Surgery
198d
Cleared
Nov 21, 2007
MONOJECT HYPODERMIC NEEDLE, MODEL 250, 30 GAUGE HYPODERMIC NEEDLE
General Hospital
15d