LIGHT, HEAD, EXAMINATION— 510(k) K901706

Name: FDA 510(k) clearance K901706
Creator: U.S. Food and Drug Administration
Published: 1990-07-19

Substantially Equivalent

Burton Medical Products Corp.

FDA 510(k) clearance K901706 for LIGHT, HEAD, EXAMINATION, Substantially Equivalent on 1990-07-19. Applicant: Burton Medical Products Corp.. Device class: 1.

Clearance details

Applicant: Burton Medical Products Corp.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1990-04-12
Decision date: 1990-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Van Nuys, CA, US

Download summary PDF View on FDA.gov ↗

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