CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT— 510(k) K063235

Substantially Equivalent

Cytori Therapeutics, Inc.

FDA 510(k) clearance K063235 for CYTORI LIPOPLASTY SYSTEM WITH CELASE REAGENT, Substantially Equivalent on 2007-01-24. Applicant: Cytori Therapeutics, Inc.. Device class: 2.

Clearance details

Applicant
Cytori Therapeutics, Inc.
Product code
Code QPB
Device class
Class 2
Regulation
21 CFR 878.5040
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Diego, CA, US
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