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FDA 510(k) Application Details - K052322
Device Classification Name
Mesh, Surgical
More FDA Info for this Device
510(K) Number
K052322
Device Name
Mesh, Surgical
Applicant
C.R. BARD, INC.
100 SOCKANOSSETT CROSSROAD
P.O. BOX 8500
CRANSTON, RI 02920 US
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Contact
ROBIN DRAGO
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Regulation Number
878.3300
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Classification Product Code
FTM
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More FDA Info for this Product Code
Date Received
08/25/2005
Decision Date
04/10/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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