DXS DIGITAL X-RAY SYSTEM
K-Number: K013271 · 2001-12-13
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Device Summary
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
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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