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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameMODEL 4553 DUAL CHAM. DDD TEMP.CARDIAC PACEMAKER
Classification Namegenerator, pulse, pacemaker, external programmable
Generic Namepacemaker
Regulation Number870.1750
ApplicantPACE MEDICAL
PMA NumberP920032
Supplement NumberS001
Date Received12/06/1994
Decision Date08/28/1995
Product Code
JOQ[ Registered Establishments with JOQ ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - other
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the micro-pace models 4570, 4573, & 4575 dual chamber ddd temporary cardiac pacemakers.
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