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FDA 510(k) Application Details - K982632
Device Classification Name
Catheter, Percutaneous
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510(K) Number
K982632
Device Name
Catheter, Percutaneous
Applicant
CORDIS CORP.
14201 N.W. 60TH AVE.
MIAMI LAKES, FL 33014 US
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Contact
MARTINE D SCHNEIDER
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Regulation Number
870.1250
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Classification Product Code
DQY
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More FDA Info for this Product Code
Date Received
07/23/1998
Decision Date
08/18/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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