CYTORI PUREGRAFT 250/PURE SYSTEM— 510(k) K092923

Substantially Equivalent

Cytori Therapeutics, Inc.

FDA 510(k) clearance K092923 for CYTORI PUREGRAFT 250/PURE SYSTEM, Substantially Equivalent on 2010-01-06. Applicant: Cytori Therapeutics, Inc..

Clearance details

Applicant: Cytori Therapeutics, Inc.
Product code: Code MUU
Advisory panel: General, Plastic Surgery
Date received: 2009-09-23
Decision date: 2010-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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