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FDA 510(k) Application Details - K063235
Device Classification Name
More FDA Info for this Device
510(K) Number
K063235
Device Name
CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT
Applicant
CYTORI THERAPEUTICS, INC.
3020 CALLAN ROAD
SAN DIEGO, CA 92121-1109 US
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Contact
KENNETH K KLEINHENZ
Other 510(k) Applications for this Contact
Regulation Number
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Classification Product Code
QPB
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More FDA Info for this Product Code
Date Received
10/25/2006
Decision Date
01/24/2007
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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