AUTO REF-KERATOMETER, RK-3— 510(k) K942242

Substantially Equivalent

Cannon U.S.A., Inc.

FDA 510(k) clearance K942242 for AUTO REF-KERATOMETER, RK-3, Substantially Equivalent on 1994-09-02. Applicant: Cannon U.S.A., Inc.. Device class: 1.

Clearance details

Applicant: Cannon U.S.A., Inc.
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 1994-05-09
Decision date: 1994-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Success, NY, US

Download summary PDF View on FDA.gov ↗

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