OCCU-TECH VISION TEST— 510(k) K881971

Name: FDA 510(k) clearance K881971
Creator: U.S. Food and Drug Administration
Published: 1988-11-25

Substantially Equivalent

Applied Vision Concepts, Inc.

FDA 510(k) clearance K881971 for OCCU-TECH VISION TEST, Substantially Equivalent on 1988-11-25. Applicant: Applied Vision Concepts, Inc.. Device class: 1.

Clearance details

Applicant: Applied Vision Concepts, Inc.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 1988-05-11
Decision date: 1988-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

Download summary PDF View on FDA.gov ↗

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