KELVIN (R) PACING SYSTEM

Implantable Pacemaker Pulse-generator

FDA Premarket Approval P870054 S011

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 (R) PACING SYSTEM
Classification NameImplantable Pacemaker Pulse-generator
Generic NameImplantable Pacemaker Pulse-generator
ApplicantCOOK PACEMAKER CORP.
Date Received1990-03-05
Decision Date1990-03-19
PMAP870054
SupplementS011
Product CodeDXY
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonOther Report
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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