KELVIN MODEL 500 UNIPOLAR CARDIAC PULSE GENERATOR

Implantable Pacemaker Pulse-generator

FDA Premarket Approval P870054

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

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 Received1987-09-08
Decision Date1988-04-29
Notice Date1988-06-09
PMAP870054
SupplementS
Product CodeDXY
Docket Number88M-0187
Advisory CommitteeCardiovascular
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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