KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR

Implantable Pacemaker Pulse-generator

FDA Premarket Approval P870054 S001

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceKELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR
Classification NameImplantable Pacemaker Pulse-generator
Generic NameImplantable Pacemaker Pulse-generator
ApplicantCOOK PACEMAKER CORP.
Date Received1988-11-10
Decision Date1989-03-29
PMAP870054
SupplementS001
Product CodeDXY
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address COOK PACEMAKER CORP. route 66 River Rd. p.o. Box 529 leechburg, PA 15656

Supplemental Filings

Supplement NumberDateSupplement Type
P870054Original Filing
S014 1995-06-08 Normal 180 Day Track
S013
S012
S011 1990-03-05 Normal 180 Day Track
S010 1990-02-23 Normal 180 Day Track
S009 1989-12-20 Normal 180 Day Track
S008
S007
S006 1989-04-25 Normal 180 Day Track
S005 1989-03-06 Normal 180 Day Track
S004 1989-02-13 Normal 180 Day Track
S003 1989-01-23 Normal 180 Day Track
S002 1989-01-17 Normal 180 Day Track
S001 1988-11-10 Normal 180 Day Track

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