OPTEC 1000 DMV VISION TESTER MODIFY— 510(k) K875237

Name: FDA 510(k) clearance K875237
Creator: U.S. Food and Drug Administration
Published: 1988-03-17

Substantially Equivalent

Stereo Optical Co., Inc.

FDA 510(k) clearance K875237 for OPTEC 1000 DMV VISION TESTER MODIFY, Substantially Equivalent on 1988-03-17. Applicant: Stereo Optical Co., Inc.. Device class: 1.

Clearance details

Applicant: Stereo Optical Co., Inc.
Product code: Code HOX
Device class: Class 1
Regulation: 21 CFR 886.1150
Advisory panel: Ophthalmic
Date received: 1987-12-22
Decision date: 1988-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, 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.