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FDA 510(k)

VESTIBULAR ANALYSIS APPARATUS

K-Number: K121590 · 2012-09-20

Decision Date2012-09-20
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

VESTIBULAR ANALYSIS APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Capacity Sports, LLC. It received FDA 510(k) clearance on 2012-09-20 under 510(k) number K121590. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESTIBULAR ANALYSIS APPARATUS?

VESTIBULAR ANALYSIS APPARATUS is a medical device that received FDA 510(k) clearance on 2012-09-20. The listed applicant is Capacity Sports, LLC. The 510(k) number is K121590.

When did VESTIBULAR ANALYSIS APPARATUS receive FDA 510(k) clearance?

VESTIBULAR ANALYSIS APPARATUS received FDA 510(k) clearance on 2012-09-20, under 510(k) number K121590.

Who is the listed applicant for VESTIBULAR ANALYSIS APPARATUS?

The FDA 510(k) record lists Capacity Sports, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VESTIBULAR ANALYSIS APPARATUS?

The FDA product code for VESTIBULAR ANALYSIS APPARATUS 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.

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

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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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