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FDA 510(k) Application Details - K152136
Device Classification Name
Device, Percutaneous Retrieval
More FDA Info for this Device
510(K) Number
K152136
Device Name
Device, Percutaneous Retrieval
Applicant
C.R. Bard, Inc.
1625 West Third Street
Tempe, AZ 85281 US
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Contact
Joni Creal
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
07/31/2015
Decision Date
02/18/2016
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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