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

BIOTRONIK D2K UNIPOLAR PE-60/4

K Number: K833104 · Decision Oct 19, 1983
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
41
Review Days
37

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Basic Information

Device Name
BIOTRONIK D2K UNIPOLAR PE-60/4
K Number
K833104
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Biotronik Sales, Inc.
Date Received
September 12, 1983
Decision Date
October 19, 1983
Product Code
DTB
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
DTB Permanent Pacemaker Electrode

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DTB), ordered by most recent decision date.

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Other Clearances by Biotronik Sales, Inc.

K Number Device Name
K875199 NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR
K853194 ERA-20
K860036 EDP-20 PACEMAKER
K863879 NEOS-M VS-1 PULSE GENERATOR
K863878 TRIOS-M VS-1 PULSE GENERATOR
K863480 BIOTRONIK PERMANENT PACEMAKER ELECTRODE
K860921 NEOS VS-1, PULSE GENERATOR
K860922 MIKROS, MIKROS VS-1, PULSE GENERATOR
K853567 DJP UNIPOLAR
K853566 DJ UNIPOLAR
Search all 41 clearances from Biotronik Sales, Inc. →