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FDA 510(k)

VESTIBULAR AUTOROTATION TEST

K-Number: K871466 · 1987-07-24

ApplicantWestern Systems Research, Inc.
Decision Date1987-07-24
Product CodeGWN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VESTIBULAR AUTOROTATION TEST is the device name listed in this FDA 510(k) record. The listed applicant is Western Systems Research, Inc.. It received FDA 510(k) clearance on 1987-07-24 under 510(k) number K871466. The device is classified under product code GWN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESTIBULAR AUTOROTATION TEST?

VESTIBULAR AUTOROTATION TEST is a medical device that received FDA 510(k) clearance on 1987-07-24. The listed applicant is Western Systems Research, Inc.. The 510(k) number is K871466.

When did VESTIBULAR AUTOROTATION TEST receive FDA 510(k) clearance?

VESTIBULAR AUTOROTATION TEST received FDA 510(k) clearance on 1987-07-24, under 510(k) number K871466.

Who is the listed applicant for VESTIBULAR AUTOROTATION TEST?

The FDA 510(k) record lists Western Systems Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VESTIBULAR AUTOROTATION TEST?

The FDA product code for VESTIBULAR AUTOROTATION TEST is GWN.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Western Systems Research, 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.

K010059ENGPLUS

Related Devices (Code: GWN)

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.

K260566SMARTVERTIGO™ Vestibular Assessment SystemVertigoDx, Inc.K243709NeuroEars-Anna™Neuroears, Inc.K242198ICS Dizcovery (1091)Natus Medical Denmark ApsK242726Synapsys VHITInventis S.R.L.K223047NeuroSwift ProNeurobit Technologies Co., Ltd.K203082Insight Infrared Video GogglesVestibular First

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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