ClearanceBrief
Company ยท US

Cytori Therapeutics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2014. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MUUSystem, Suction, Lipoplasty4
CACApparatus, Autotransfusion1
QPBSystem, Suction, Lipoplasty For Removal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 24, 2014K132815PUREGRAFT 50 SYSTEM
Cytori Therapeutics, Inc.
MUU
Mar 7, 2012K113255PUREGRAFT 850/PURE SYSTEM
Cytori Therapeutics, Inc.
MUU
Jan 6, 2010K092923CYTORI PUREGRAFT 250/PURE SYSTEM
Cytori Therapeutics, Inc.
MUU
Dec 10, 2007K072587CYTORI AFT SYSTEM
Cytori Therapeutics, Inc.
MUU
Jan 24, 2007K063235CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT
Cytori Therapeutics, Inc.
QPB
Sep 28, 2006K060482CYTORI CELUTION CELL CONCENTRATION DEVICE
Cytori Therapeutics, Inc.
CAC

Latest recalls

DateFirm and productCodeLinked 510(k)
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