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FDA 510(k)

MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE

K-Number: K896024 · 1990-01-22

Decision Date1990-01-22
Product CodeEAP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Diagnostic Co.. It received FDA 510(k) clearance on 1990-01-22 under 510(k) number K896024. The device is classified under product code EAP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE?

MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Mdt Diagnostic Co.. The 510(k) number is K896024.

When did MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE receive FDA 510(k) clearance?

MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE received FDA 510(k) clearance on 1990-01-22, under 510(k) number K896024.

Who is the listed applicant for MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE?

The FDA 510(k) record lists Mdt Diagnostic Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE?

The FDA product code for MDT/CASTLE MODEL HDX DENTAL X-RAY MACHINE is EAP.

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: EAP)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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