MEDUS GMBH— 510(k) K853153

Substantially Equivalent

Corkes Medical Co.

FDA 510(k) clearance K853153 for MEDUS GMBH, Substantially Equivalent on 1985-08-07. Applicant: Corkes Medical Co.. Device class: 1.

Clearance details

Applicant: Corkes Medical Co.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-07-29
Decision date: 1985-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, 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.