MICROLIGHT 830 LASER SYSTEM— 510(k) K010175

Name: FDA 510(k) clearance K010175
Creator: U.S. Food and Drug Administration
Published: 2002-02-06

Substantially Equivalent

Microlight Corporation of America

FDA 510(k) clearance K010175 for MICROLIGHT 830 LASER SYSTEM, Substantially Equivalent on 2002-02-06. Applicant: Microlight Corporation of America. Device class: 2.

Clearance details

Applicant: Microlight Corporation of America
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2001-01-18
Decision date: 2002-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Missouri City, TX, US

Download summary PDF View on FDA.gov ↗

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