VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)— 510(k) K891008

Name: FDA 510(k) clearance K891008
Creator: U.S. Food and Drug Administration
Published: 1989-05-31

Substantially Equivalent

Micromedical Technologies, Inc.

FDA 510(k) clearance K891008 for VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ), Substantially Equivalent on 1989-05-31. Applicant: Micromedical Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Micromedical Technologies, Inc.
Product code: Code LXV
Device class: Unclassified
Advisory panel: Unknown
Date received: 1989-03-03
Decision date: 1989-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatham, 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.