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FDA 510(k)

DXS DIGITAL X-RAY SYSTEM

K-Number: K013271 · 2001-12-13

Decision Date2001-12-13
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DXS DIGITAL X-RAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Douglas C. Yoon, Dds. It received FDA 510(k) clearance on 2001-12-13 under 510(k) number K013271. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DXS DIGITAL X-RAY SYSTEM?

DXS DIGITAL X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2001-12-13. The listed applicant is Douglas C. Yoon, Dds. The 510(k) number is K013271.

When did DXS DIGITAL X-RAY SYSTEM receive FDA 510(k) clearance?

DXS DIGITAL X-RAY SYSTEM received FDA 510(k) clearance on 2001-12-13, under 510(k) number K013271.

Who is the listed applicant for DXS DIGITAL X-RAY SYSTEM?

The FDA 510(k) record lists Douglas C. Yoon, Dds as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DXS DIGITAL X-RAY SYSTEM?

The FDA product code for DXS DIGITAL X-RAY SYSTEM is MUH.

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: MUH)

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

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