CYTORI AFT SYSTEM— 510(k) K072587

Substantially Equivalent

Cytori Therapeutics, Inc.

FDA 510(k) clearance K072587 for CYTORI AFT SYSTEM, Substantially Equivalent on 2007-12-10. Applicant: Cytori Therapeutics, Inc.. Device class: 2.

Clearance details

Applicant: Cytori Therapeutics, Inc.
Product code: Code MUU
Device class: Class 2
Regulation: 21 CFR 878.5040
Advisory panel: General, Plastic Surgery
Date received: 2007-09-14
Decision date: 2007-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.