Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING

K-Number: K872093 · 1987-09-16

Decision Date1987-09-16
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING is the device name listed in this FDA 510(k) record. The listed applicant is Ics Medical Corp.. It received FDA 510(k) clearance on 1987-09-16 under 510(k) number K872093. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING?

RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Ics Medical Corp.. The 510(k) number is K872093.

When did RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING receive FDA 510(k) clearance?

RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING received FDA 510(k) clearance on 1987-09-16, under 510(k) number K872093.

Who is the listed applicant for RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING?

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

What is the FDA product code for RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING?

The FDA product code for RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING 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 Ics Medical Corp. 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.

View all 10 devices →

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.

↑