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FDA 510(k) Applications Submitted by CYTORI THERAPEUTICS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K072587
09/14/2007
CYTORI AFT SYSTEM
CYTORI THERAPEUTICS, INC.
K060482
02/23/2006
CYTORI CELUTION CELL CONCENTRATION DEVICE
CYTORI THERAPEUTICS, INC.
K132815
09/09/2013
PUREGRAFT 50 SYSTEM
CYTORI THERAPEUTICS, INC.
K092923
09/23/2009
CYTORI PUREGRAFT 250/PURE SYSTEM
CYTORI THERAPEUTICS, INC.
K063235
10/25/2006
CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT
CYTORI THERAPEUTICS, INC.
K113255
11/03/2011
PUREGRAFT 850/PURE SYSTEM
CYTORI THERAPEUTICS, INC.
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