AUTOREF LENSMETER RL-10— 510(k) K925304

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K925304 for AUTOREF LENSMETER RL-10, Substantially Equivalent on 1994-02-17. Applicant: Canon USA, Inc.. Device class: 1.

Clearance details

Applicant: Canon USA, Inc.
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 1992-10-21
Decision date: 1994-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo 146, JP

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.