Estech, Inc. is one of 5166 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Estech, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Estech, Inc. has 7 FDA 510(k) cleared medical devices. Based in Danville, US.
Historical record: 7 cleared submissions from 1999 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Estech, Inc. Filter by specialty or product code using the sidebar.
Estech, Inc. — FDA 510(k) Products and Clearance History
7 devices
Cleared
Oct 07, 2013
ESTECH COBRA(R) GENESIS BIPOLAR CLAMP
General & Plastic Surgery
11d
Cleared
Jan 26, 2006
ESTECH CLEARVIEW MV ATRIAL DEPRESSOR
Cardiovascular
92d
Cleared
Dec 16, 2005
REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULA
Cardiovascular
136d
Cleared
Sep 13, 2005
COBRA SURGICAL SYSTEM
General & Plastic Surgery
76d
Cleared
Jul 27, 2004
COBRA ADHERE SURGICAL SYSTEM
General & Plastic Surgery
43d
Cleared
Oct 22, 2003
REMOTE ACCESS PERFUSION CANNULA LEFT AXILLARY 21 FRENCH
Cardiovascular
57d
Cleared
Mar 11, 1999
ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULA
Cardiovascular
16d