FDA Device Entity Profile: Covidien, Formerly US Surgical A Divison of Tyco H

Known Identifiers & Locations

FEI Numbers N/A

Owner Operator Numbers N/A

Locations Covered N/A

Registered Establishments (0)

No device registration and listing records found for this entity.

510(k) Premarket Notifications (5)

Submission #	Device Name	Decision Date	Decision Description	Action
K103263	ENDO GIA SINGLEUSE DUET TRS RELOAD WITH TRI0STAPLE TECHNOLOGY	2010-11-22	Substantially Equivalent	View Details
K112349	VERSAPORT V2 BLADELESS OPTIICAL TROCAR AND/OR VERSAPORT BLADELESS OPTICAL TROCAR	2011-09-01	Substantially Equivalent	View Details
K120061	WOUND PROTECTOR	2012-03-27	Substantially Equivalent	View Details
K130717	ENDO GIA RELOAD	2013-04-18	Substantially Equivalent	View Details
K131705	ENDO GIA RADIAL RELOAD WITH TRI-STAPLE TECHNOLOGY	2013-07-01	Substantially Equivalent	View Details

FDA Recall History (0)

No recall records found for this entity.

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