MINNESOTA SCIENTIFIC, INC. OMNI-BEAM— 510(k) K853948

Name: FDA 510(k) clearance K853948
Creator: U.S. Food and Drug Administration
Published: 1985-10-16

Substantially Equivalent

Minnesota Scientific, Inc.

FDA 510(k) clearance K853948 for MINNESOTA SCIENTIFIC, INC. OMNI-BEAM, Substantially Equivalent on 1985-10-16. Applicant: Minnesota Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Minnesota Scientific, Inc.
Product code: Code HBI
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1985-09-24
Decision date: 1985-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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