UROLIX-3 UROLOGICAL TABLE
K-Number: K840227 · 1984-03-23
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Device Summary
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.
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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