Biotronik, GmbH & Co. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biotronik, GmbH & Co. Cardiovascular ✕
18 devices
Cleared
Apr 06, 2000
PX 53/15-BP, MODEL 130 050 AND PX 60/15-BP, MODEL 130 051
Cardiovascular
28d
Cleared
Sep 22, 1993
BIOSCOPE
Cardiovascular
439d
Cleared
Aug 19, 1993
PIKOS 01-A AND PIKOS E01-A IMPLANTABLE PACEMAKER
Cardiovascular
422d
Cleared
Mar 18, 1993
HPM 40 HEART PACEMAKER MONITOR
Cardiovascular
283d
Cleared
Feb 26, 1992
PIKOS 01 & PIKOS E 01
Cardiovascular
166d
Cleared
Aug 28, 1991
PERMANENT IMPLANTABLE JP ENDOCARDIAL LEADS W/TIP
Cardiovascular
197d
Cleared
Aug 09, 1991
LEAD TERMINAL PIN CAPS, VARIOUS MODELS
Cardiovascular
148d
Cleared
Jul 30, 1991
PERMANENT IMPLANTABLE FH ENDOCARDIAL LEADS W/TIP
Cardiovascular
168d
Cleared
May 07, 1991
TRIOS 02
Cardiovascular
175d
Cleared
Oct 16, 1990
LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD, DJP 45-UP
Cardiovascular
57d
Cleared
Oct 16, 1990
LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD DJP 53-UP
Cardiovascular
57d
Cleared
Oct 16, 1990
LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD, DJP 60-UP
Cardiovascular
57d