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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