Cytori Therapeutics, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Cytori Therapeutics, Inc. has 6 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 6 cleared submissions from 2006 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cytori Therapeutics, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jan 24, 2014
PUREGRAFT 50 SYSTEM
General & Plastic Surgery
137d
Cleared
Mar 07, 2012
PUREGRAFT 850/PURE SYSTEM
General & Plastic Surgery
125d
Cleared
Jan 06, 2010
CYTORI PUREGRAFT 250/PURE SYSTEM
General & Plastic Surgery
105d
Cleared
Dec 10, 2007
CYTORI AFT SYSTEM
General & Plastic Surgery
87d
Cleared
Jan 24, 2007
CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT
General & Plastic Surgery
91d
Cleared
Sep 28, 2006
CYTORI CELUTION CELL CONCENTRATION DEVICE
Anesthesiology
217d