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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Trade NameCORDIS SEQUICOR THETA MODELS 233D & 233E
Classification Nameimplantable pulse generator, pacemaker (non-crt)
Generic Namedual chamber, implantable pulse generator
ApplicantTPL-CORDIS, INC.
PMA NumberP820014
Supplement NumberS041
Date Received04/03/1989
Decision Date04/18/1989
Product Code
LWP[ Registered Establishments with LWP ]
Advisory Committee Anesthesiology
Supplement Typenormal 180 day track
Supplement Reason location change: sterilizer
Expedited Review Granted? No
Combination Product No
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