THERMOLYSIS GENERATOR— 510(k) K780337

Substantially Equivalent

Clare, Inc.

FDA 510(k) clearance K780337 for THERMOLYSIS GENERATOR, Substantially Equivalent on 1978-04-12. Applicant: Clare, Inc.. Device class: 1.

Clearance details

Applicant: Clare, Inc.
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1978-03-02
Decision date: 1978-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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