VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
K-Number: K891008 · 1989-05-31
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Device Summary
Frequently Asked Questions
What is the VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)?
VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ) is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is Micromedical Technologies, Inc.. The 510(k) number is K891008.
When did VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ) receive FDA 510(k) clearance?
VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ) received FDA 510(k) clearance on 1989-05-31, under 510(k) number K891008.
Who is the listed applicant for VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)?
The FDA 510(k) record lists Micromedical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)?
The FDA product code for VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ) is LXV.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Micromedical Technologies, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LXV)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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