WEINGART MODEL 1000 SUNLAMP PRODUCT— 510(k) K863518

Name: FDA 510(k) clearance K863518
Creator: U.S. Food and Drug Administration
Published: 1986-10-02

Substantially Equivalent

Weingart, Inc.

FDA 510(k) clearance K863518 for WEINGART MODEL 1000 SUNLAMP PRODUCT, Substantially Equivalent on 1986-10-02. Applicant: Weingart, Inc.. Device class: 2.

Clearance details

Applicant: Weingart, Inc.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1986-09-09
Decision date: 1986-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ft Wayne, IN, US

Download summary PDF View on FDA.gov ↗

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