Biotronik, GmbH & Co.
Biotronik, GmbH & Co. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2000.
Top product codes for Biotronik, GmbH & Co.
Recent clearances by Biotronik, GmbH & Co.
- K000763 — PX 53/15-BP, MODEL 130 050 AND PX 60/15-BP, MODEL 130 051
- K923406 — BIOSCOPE
- K923026 — PIKOS 01-A AND PIKOS E01-A IMPLANTABLE PACEMAKER
- K922742 — HPM 40 HEART PACEMAKER MONITOR
- K914109 — PIKOS 01 & PIKOS E 01
- K910609 — PERMANENT IMPLANTABLE JP ENDOCARDIAL LEADS W/TIP
- K911142 — LEAD TERMINAL PIN CAPS, VARIOUS MODELS
- K910608 — PERMANENT IMPLANTABLE FH ENDOCARDIAL LEADS W/TIP
- K905087 — TRIOS 02
- K903927 — LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD, DJP 45-UP
- K903928 — LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD DJP 53-UP
- K903929 — LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD, DJP 60-UP
- K903081 — NEOS (TM) 02 B PULSE GENERATOR
- K902889 — A1-A,A1-B,A1-ABP,A1-MBP,A1-Z,A6-A,A6-B,PEH PACE.
- K896824 — BIOTRONIK'S PS-ENDOCARDIAL LEADS
- K901709 — DNP 60-B UNIPOLAR ENDOCARDIAL LEAD
- K901332 — PK-55 ANDOVER MEDICAL PART #5455 LABEL CHANGE
- K894494 — LABELING CHANGES TO PULSE GENE. & PULSE GENE. LEAD
Data sourced from openFDA. This site is unofficial and independent of the FDA.