Cordis Leads, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cordis Leads, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cordis Leads, Inc. has 4 FDA 510(k) cleared medical devices. Based in Suffield, US.
Historical record: 4 cleared submissions from 1988 to 1988. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cordis Leads, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cordis Leads, Inc.
4 devices
Cleared
Dec 05, 1988
ENCOR UNIPOLAR VS-1 LEADS
Cardiovascular
138d
Cleared
Oct 19, 1988
CHANGES TO ENCOR PERVENOUS J-ATRIAL LEADS
Cardiovascular
399d
Cleared
Jul 12, 1988
HIGH TORQUE TEMPORARY PERVENOUS LEAD W/DEPTH MARK
Cardiovascular
57d
Cleared
Jun 16, 1988
ENCOR BIPOLAR ACT/FIXA LEAD W/POR SUR ELE #329-201
Cardiovascular
237d