CENTRAL VISION ANALYZER MODEL 1000— 510(k) K100095

Name: FDA 510(k) clearance K100095
Creator: U.S. Food and Drug Administration
Published: 2010-05-10

Substantially Equivalent

Vimetrics,Llc.

FDA 510(k) clearance K100095 for CENTRAL VISION ANALYZER MODEL 1000, Substantially Equivalent on 2010-05-10. Applicant: Vimetrics,Llc.. Device class: 1.

Clearance details

Applicant: Vimetrics,Llc.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 2010-01-13
Decision date: 2010-05-10
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Media, PA, US

Download summary PDF View on FDA.gov ↗

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