EUROSUN MODELS - ES-2400, ES-VHO AND ES-16— 510(k) K904644

Name: FDA 510(k) clearance K904644
Creator: U.S. Food and Drug Administration
Published: 1990-12-28

Substantially Equivalent

Eurosun, Inc.

FDA 510(k) clearance K904644 for EUROSUN MODELS - ES-2400, ES-VHO AND ES-16, Substantially Equivalent on 1990-12-28. Applicant: Eurosun, Inc.. Device class: 2.

Clearance details

Applicant: Eurosun, Inc.
Product code: Code LEJ
Device class: Class 2
Regulation: 21 CFR 878.4635
Advisory panel: General, Plastic Surgery
Date received: 1990-10-11
Decision date: 1990-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Huntington, WV, US

Download summary PDF View on FDA.gov ↗

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