FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

NEOS (TM) 02 B PULSE GENERATOR

K Number: K903081 · Decision Sep 14, 1990
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
460
Applicant Total
18
Review Days
64

Basic Information

Device Name
NEOS (TM) 02 B PULSE GENERATOR
K Number
K903081
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
BIOTRONIK, GMBH & CO.
Date Received
July 12, 1990
Decision Date
September 14, 1990
Product Code
DXY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXY Implantable Pacemaker Pulse-Generator

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Other Clearances by BIOTRONIK, GMBH & CO.

K Number Device Name
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
K903928 LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD DJP 53-UP
Search all 18 clearances from BIOTRONIK, GMBH & CO. →