NON-MYDRIATIC RETINAL CAMERA— 510(k) K941234

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K941234 for NON-MYDRIATIC RETINAL CAMERA, Substantially Equivalent on 1995-06-07. Applicant: Canon USA, Inc.. Device class: 2.

Clearance details

Applicant: Canon USA, Inc.
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 1994-03-15
Decision date: 1995-06-07
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.