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

BIFOCAL 2 8200 SERIES (A,B C,D)

K Number: K800379 · Decision Sep 26, 1980
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
460
Applicant Total
14
Review Days
217

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Basic Information

Device Name
BIFOCAL 2 8200 SERIES (A,B C,D)
K Number
K800379
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
American Pacemaker Corp.
Date Received
February 22, 1980
Decision Date
September 26, 1980
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

Similar 510(k) Clearances

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

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Other Clearances by American Pacemaker Corp.

K Number Device Name
K821791 EXTERNAL PULSE GENERATOR - EV4542
K812830 APC IMPLANTABLE PACING LEAD
K812807 APC IMPLANTABLE PACING LEADS
K810397 APC IMPLANTABLE PACING LEAD-FLANGE #3260
K810396 APC IMPLANTABLE PACING LEAD, TINED #3262
K810398 APC IMPLANTABLE PACING LEAD, MODEL 3266
K810399 APC IMPLANTABEL PACING LEAD, MODEL 3264
K810121 UNIFOCAL 3
K800746 UNIFOCAL VP, MODELS 7501 AND 7502
K791955 UNIFOCAL 1 UNIPOLAR DEMAND R WAVE
Search all 14 clearances from American Pacemaker Corp. →