CANON SURGICAL AUTO KERATOMETER SK-1— 510(k) K871936

Name: FDA 510(k) clearance K871936
Creator: U.S. Food and Drug Administration
Published: 1987-06-19

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K871936 for CANON SURGICAL AUTO KERATOMETER SK-1, Substantially Equivalent on 1987-06-19. Applicant: Canon USA, Inc.. Device class: 1.

Clearance details

Applicant: Canon USA, Inc.
Product code: Code HLQ
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1987-05-18
Decision date: 1987-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jericho, NY, US

Download summary PDF View on FDA.gov ↗

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