FLOOR STANDING, OPERATING AND EXAMINING LIGHT— 510(k) K893813

Name: FDA 510(k) clearance K893813
Creator: U.S. Food and Drug Administration
Published: 1989-07-14

Substantially Equivalent

Astralite Corp.

FDA 510(k) clearance K893813 for FLOOR STANDING, OPERATING AND EXAMINING LIGHT, Substantially Equivalent on 1989-07-14. Applicant: Astralite Corp.. Device class: 2.

Clearance details

Applicant: Astralite Corp.
Product code: Code FSS
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1989-05-23
Decision date: 1989-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Diamond Springs, CA, US

Download summary PDF View on FDA.gov ↗

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