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FDA 510(k)

MEDIADENT HDX/MMD HDX SP XRAY SENSOR

K-Number: K002425 · 2000-12-21

ApplicantMulti Media Dental Systems, Inc.
Decision Date2000-12-21
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEDIADENT HDX/MMD HDX SP XRAY SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Multi Media Dental Systems, Inc.. It received FDA 510(k) clearance on 2000-12-21 under 510(k) number K002425. 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 MEDIADENT HDX/MMD HDX SP XRAY SENSOR?

MEDIADENT HDX/MMD HDX SP XRAY SENSOR is a medical device that received FDA 510(k) clearance on 2000-12-21. The listed applicant is Multi Media Dental Systems, Inc.. The 510(k) number is K002425.

When did MEDIADENT HDX/MMD HDX SP XRAY SENSOR receive FDA 510(k) clearance?

MEDIADENT HDX/MMD HDX SP XRAY SENSOR received FDA 510(k) clearance on 2000-12-21, under 510(k) number K002425.

Who is the listed applicant for MEDIADENT HDX/MMD HDX SP XRAY SENSOR?

The FDA 510(k) record lists Multi Media Dental Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIADENT HDX/MMD HDX SP XRAY SENSOR?

The FDA product code for MEDIADENT HDX/MMD HDX SP XRAY SENSOR 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.

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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.

K251793SOTA Cloud Smart Sensor (1.5)Sota Cloud Corp.K252570EzSensor HD, EzSensor UHDQpix Solutions, Inc.K250687Cocoon Solo (DX-7020s)Dexcowin Global, Inc.K251206Digital X-Ray DentiMax Pro Imaging SystemDentimax, Inc.K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)VATECH Co., Ltd.K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)Qpix Solutions, Inc.

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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