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FDA 510(k)

UROLIX-3 UROLOGICAL TABLE

K-Number: K840227 · 1984-03-23

Decision Date1984-03-23
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UROLIX-3 UROLOGICAL TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840227. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROLIX-3 UROLOGICAL TABLE?

UROLIX-3 UROLOGICAL TABLE is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K840227.

When did UROLIX-3 UROLOGICAL TABLE receive FDA 510(k) clearance?

UROLIX-3 UROLOGICAL TABLE received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840227.

Who is the listed applicant for UROLIX-3 UROLOGICAL TABLE?

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

What is the FDA product code for UROLIX-3 UROLOGICAL TABLE?

The FDA product code for UROLIX-3 UROLOGICAL TABLE is IXR.

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 Medicor USA , Ltd. 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 14 devices →

Related Devices (Code: IXR)

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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