CANON AUTO REF-KERATOMETER RK-2— 510(k) K895475

Name: FDA 510(k) clearance K895475
Creator: U.S. Food and Drug Administration
Published: 1989-10-31

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K895475 for CANON AUTO REF-KERATOMETER RK-2, Substantially Equivalent on 1989-10-31. 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: 1989-09-11
Decision date: 1989-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo 146, JP

Download summary PDF View on FDA.gov ↗

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