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FDA 510(k) Application Details - DEN110004
Device Classification Name
More FDA Info for this Device
510(K) Number
DEN110004
Device Name
CABOCHON SYSTEM
Applicant
CABOCHON AESTHETICS, INC.
127 Independence Drive
Menlo Park, CA 94025 US
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BEN BRIAN
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
OUP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/31/2011
Decision Date
07/12/2013
Decision
DENG -
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type
Post-NSE
Reviewed By Third Party
N
Expedited Review
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