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FDA 510(k)

FLOOR MOUNTED X-RAY TUBESTAND

K-Number: K843335 · 1984-11-27

Decision Date1984-11-27
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FLOOR MOUNTED X-RAY TUBESTAND 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 1984-11-27 under 510(k) number K843335. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOOR MOUNTED X-RAY TUBESTAND?

FLOOR MOUNTED X-RAY TUBESTAND is a medical device that received FDA 510(k) clearance on 1984-11-27. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K843335.

When did FLOOR MOUNTED X-RAY TUBESTAND receive FDA 510(k) clearance?

FLOOR MOUNTED X-RAY TUBESTAND received FDA 510(k) clearance on 1984-11-27, under 510(k) number K843335.

Who is the listed applicant for FLOOR MOUNTED X-RAY TUBESTAND?

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 FLOOR MOUNTED X-RAY TUBESTAND?

The FDA product code for FLOOR MOUNTED X-RAY TUBESTAND is IYB.

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: IYB)

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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