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

TRIOS 02

K Number: K905087 · Decision May 7, 1991
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
460
Applicant Total
18
Review Days
175

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Basic Information

Device Name
TRIOS 02
K Number
K905087
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Biotronik, GmbH & Co.
Date Received
November 13, 1990
Decision Date
May 7, 1991
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
K903928 LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD DJP 53-UP
K903929 LABEL CHANGE UNIPOLAR ENDOCARDIAL LEAD, DJP 60-UP
Search all 18 clearances from Biotronik, GmbH & Co. →