CANON NON-MYDRIATIC RETINAL CAMERA CR3-45NM— 510(k) K855170

Name: FDA 510(k) clearance K855170
Creator: U.S. Food and Drug Administration
Published: 1986-02-27

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K855170 for CANON NON-MYDRIATIC RETINAL CAMERA CR3-45NM, Substantially Equivalent on 1986-02-27. 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: 1985-12-26
Decision date: 1986-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jericho, NY, US

Download summary PDF View on FDA.gov ↗

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