ENDOCARDIAL PACEMAKER LEAD W/CARBON TIP

FDA Premarket Approval P800041 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

DeviceENDOCARDIAL PACEMAKER LEAD W/CARBON TIP
Generic NamePermanent Pacemaker Electrode
ApplicantPACESETTER SYSTEMS
Date Received1982-12-17
Decision Date1983-01-27
PMAP800041
SupplementS001
Product CodeDTB 
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonOther Report
Expedited ReviewNo
Combination Product No
Applicant Address PACESETTER SYSTEMS 15900 Valleyview Court p.o. Box 9221 sylmar, CA 91392-9221

Supplemental Filings

Supplement NumberDateSupplement Type
P800041Original Filing
S015 1995-10-02 Normal 180 Day Track
S014 1993-11-26 Normal 180 Day Track
S013
S012 1992-02-11 Normal 180 Day Track
S011 1991-03-29 Normal 180 Day Track
S010 1990-10-24 Special (immediate Track)
S009 1990-03-14 Normal 180 Day Track
S008 1989-05-19 Normal 180 Day Track
S007 1987-01-09 Normal 180 Day Track
S006 1986-08-12 Normal 180 Day Track
S005 1985-10-17
S004
S003 1984-11-19
S002 1983-08-18
S001 1982-12-17 Normal 180 Day Track

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