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FDA 510(k) Application Details - K972512
Device Classification Name
Catheter, Angioplasty, Peripheral, Transluminal
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510(K) Number
K972512
Device Name
Catheter, Angioplasty, Peripheral, Transluminal
Applicant
BOSTON SCIENTIFIC SCIMED, INC.
5905 NATHAN LN.
MINNEAPOLIS, MN 55442 US
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Contact
RON BENNETT
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Regulation Number
870.1250
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Classification Product Code
LIT
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More FDA Info for this Product Code
Date Received
07/07/1997
Decision Date
02/12/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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