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FDA 510(k)

CHAIR, VESTIBULAR, ROTARY, COMPUT.

K-Number: K781268 · 1978-08-14

ApplicantContraves
Decision Date1978-08-14
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

CHAIR, VESTIBULAR, ROTARY, COMPUT. is the device name listed in this FDA 510(k) record. The listed applicant is Contraves. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K781268. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHAIR, VESTIBULAR, ROTARY, COMPUT.?

CHAIR, VESTIBULAR, ROTARY, COMPUT. is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Contraves. The 510(k) number is K781268.

When did CHAIR, VESTIBULAR, ROTARY, COMPUT. receive FDA 510(k) clearance?

CHAIR, VESTIBULAR, ROTARY, COMPUT. received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781268.

Who is the listed applicant for CHAIR, VESTIBULAR, ROTARY, COMPUT.?

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

What is the FDA product code for CHAIR, VESTIBULAR, ROTARY, COMPUT.?

The FDA product code for CHAIR, VESTIBULAR, ROTARY, COMPUT. 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

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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