MODEL 4553 DUAL CHAM. DDD TEMP.CARDIAC PACEMAKER

FDA Premarket Approval P920032 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

Approval for the micro-pace models 4570, 4573, & 4575 dual chamber ddd temporary cardiac pacemakers

DeviceMODEL 4553 DUAL CHAM. DDD TEMP.CARDIAC PACEMAKER
Generic NameGenerator, Pulse, Pacemaker, External Programmable (for Electrophysiological Studies Only)
ApplicantPACE MEDICAL
Date Received1994-12-06
Decision Date1995-08-28
PMAP920032
SupplementS001
Product CodeJOQ 
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address PACE MEDICAL 391 Totten Pond Rd. waltham, MA 02451

Supplemental Filings

Supplement NumberDateSupplement Type
P920032Original Filing
S008 2001-08-16 Normal 180 Day Track
S007 2001-04-24 Normal 180 Day Track
S006 2001-01-18 Normal 180 Day Track
S005 1999-06-25 Normal 180 Day Track
S004 1998-01-30 Normal 180 Day Track
S003 1996-01-19 Normal 180 Day Track
S002 1995-11-27 Normal 180 Day Track
S001 1994-12-06 Normal 180 Day Track

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