Biotronik Sales, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biotronik Sales, Inc. - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
Biotronik Sales, Inc. has 41 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 41 cleared submissions from 1980 to 1988.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biotronik Sales, Inc.
41 devices
Cleared
Feb 18, 1988
NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR
Cardiovascular
62d
Cleared
Mar 11, 1987
ERA-20
Cardiovascular
589d
Cleared
Jan 12, 1987
EDP-20 PACEMAKER
Cardiovascular
371d
Cleared
Dec 10, 1986
TRIOS-M VS-1 PULSE GENERATOR
Cardiovascular
65d
Cleared
Dec 10, 1986
NEOS-M VS-1 PULSE GENERATOR
Cardiovascular
65d
Cleared
Sep 23, 1986
BIOTRONIK PERMANENT PACEMAKER ELECTRODE
Cardiovascular
14d
Cleared
Aug 08, 1986
NEOS VS-1, PULSE GENERATOR
Cardiovascular
150d
Cleared
Aug 04, 1986
MIKROS, MIKROS VS-1, PULSE GENERATOR
Cardiovascular
146d
Cleared
May 07, 1986
DJ UNIPOLAR
Cardiovascular
254d
Cleared
May 07, 1986
DJP UNIPOLAR
Cardiovascular
254d
Cleared
Jan 15, 1986
DNR UNIPOLAR
Cardiovascular
142d
Cleared
Sep 13, 1985
NEOS - M ABP
Cardiovascular
56d
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