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FDA 510(k), K891008, VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
FDA 510(k), K891008, VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
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510(K) Number: K891008
Device Name: VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
Manufacturer: MICROMEDICAL TECHNOLOGIES, INC.
Device Classification Name: apparatus, vestibular analysis
Regulation Number:
Classification Product Code: LXV
Date Received: 03/03/1989
Decision Date: 05/31/1989
Regulation Medical Specialty:
Device Name: VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
Manufacturer: MICROMEDICAL TECHNOLOGIES, INC.
Device Classification Name: apparatus, vestibular analysis
Regulation Number:
Classification Product Code: LXV
Date Received: 03/03/1989
Decision Date: 05/31/1989
Regulation Medical Specialty:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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