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FDA 510(k)

DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540

K-Number: K092537 · 2009-08-27

ApplicantToshiba America Electronic Components, Inc.
Decision Date2009-08-27
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540 is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Electronic Components, Inc.. It received FDA 510(k) clearance on 2009-08-27 under 510(k) number K092537. 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 DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540?

DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540 is a medical device that received FDA 510(k) clearance on 2009-08-27. The listed applicant is Toshiba America Electronic Components, Inc.. The 510(k) number is K092537.

When did DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540 receive FDA 510(k) clearance?

DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540 received FDA 510(k) clearance on 2009-08-27, under 510(k) number K092537.

Who is the listed applicant for DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540?

The FDA 510(k) record lists Toshiba America Electronic Components, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540?

The FDA product code for DIGITAL X-RAY SENSOR, MODEL E9539,E9505,E9502, E9540 is MUH.

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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

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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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