Thoratec Laboratories Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thoratec Laboratories Corp. - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Thoratec Laboratories Corp. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 9 cleared submissions from 1978 to 2000. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Thoratec Laboratories Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thoratec Laboratories Corp.
10 devices
Cleared
Dec 18, 2000
VECTRA (TM) VASCULAR ACCESS GRAFT-5MM DIAMETER,6MM DIAMETER AND VECTRA (TM)...
Cardiovascular
175d
Cleared
Sep 22, 2000
VASCULAR GRAFT TUNNELER-STANDARD CURVE, MID CURVE, FULL CURVE, SHORT STANDARD...
Cardiovascular
88d
Cleared
Aug 01, 1985
THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAY
General & Plastic Surgery
108d
Cleared
Dec 29, 1983
RESPIRATORY ASSESSMENT SYSTEM
Anesthesiology
69d
Cleared
Nov 28, 1983
RESPIRATORY FLOW MODULE
Anesthesiology
68d
Cleared
Aug 24, 1983
INTRAOPERATIVE AUTOTRANSFUSION SYS
Anesthesiology
100d
Cleared
Jan 05, 1983
RESPIRATORY GAS ANALYZER
Anesthesiology
54d
Cleared
Dec 09, 1982
RESPIRATORY CIRCUIT ADAPTOR
Anesthesiology
35d
Cleared
Oct 06, 1982
THORATEC GAS SAMPLING CONNECTOR
Anesthesiology
22d
Cleared
Feb 27, 1978
IMPCO DISPOSABLE AORTIC PUNCH
Cardiovascular
14d