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FDA 510(k) Application Details - K014109
Device Classification Name
Device, Percutaneous Retrieval
More FDA Info for this Device
510(K) Number
K014109
Device Name
Device, Percutaneous Retrieval
Applicant
BOSTON SCIENTIFIC, TARGET
47900 BAYSIDE PKWY.
FREMONT, CA 94538 US
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Contact
SETH A SCHULMAN
Other 510(k) Applications for this Contact
Regulation Number
870.5150
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Classification Product Code
MMX
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More FDA Info for this Product Code
Date Received
12/14/2001
Decision Date
03/12/2002
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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