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Cytori Therapeutics, Inc.

6 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
PUREGRAFT 50 SYSTEM (K132815)Cytori Therapeutics, Inc.2014-01-24
PUREGRAFT 850/PURE SYSTEM (K113255)Cytori Therapeutics, Inc.2012-03-07
CYTORI PUREGRAFT 250/PURE SYSTEM (K092923)Cytori Therapeutics, Inc.2010-01-06
CYTORI AFT SYSTEM (K072587)Cytori Therapeutics, Inc.2007-12-10
CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT (K063235)Cytori Therapeutics, Inc.2007-01-24
CYTORI CELUTION CELL CONCENTRATION DEVICE (K060482)Cytori Therapeutics, Inc.2006-09-28

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