WELCH ALLYN PREMIUM LIGHTWEIGHT HEADLIGHT— 510(k) K952691

Name: FDA 510(k) clearance K952691
Creator: U.S. Food and Drug Administration
Published: 1995-07-31

Substantially Equivalent

Welch Allyn, Inc.

FDA 510(k) clearance K952691 for WELCH ALLYN PREMIUM LIGHTWEIGHT HEADLIGHT, Substantially Equivalent on 1995-07-31. Applicant: Welch Allyn, Inc.. Device class: 2.

Clearance details

Applicant: Welch Allyn, Inc.
Product code: Code FJC
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1995-06-12
Decision date: 1995-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skaneateles Falls, NY, US

Download summary PDF View on FDA.gov ↗

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