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FDA 510(k) Application Details - K071189
Device Classification Name
Catheter, Angioplasty, Peripheral, Transluminal
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510(K) Number
K071189
Device Name
Catheter, Angioplasty, Peripheral, Transluminal
Applicant
CORDIS EUROPA, N.V.
OOSTEINDE 8
RODEN NL-9301 LJ NL
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Contact
HARM HOVINGA
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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
04/30/2007
Decision Date
05/16/2007
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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