MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR— 510(k) K900091

Name: FDA 510(k) clearance K900091
Creator: U.S. Food and Drug Administration
Published: 1990-04-04

Substantially Equivalent

Onufryk Low Vision Ent.

FDA 510(k) clearance K900091 for MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR, Substantially Equivalent on 1990-04-04. Applicant: Onufryk Low Vision Ent.. Device class: 1.

Clearance details

Applicant: Onufryk Low Vision Ent.
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1990-01-05
Decision date: 1990-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairport, NY, US

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