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FDA 510(k)

DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A

K-Number: K090742 · 2009-09-18

ApplicantSamsung Mobile Display Co., Ltd.
Decision Date2009-09-18
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A is the device name listed in this FDA 510(k) record. The listed applicant is Samsung Mobile Display Co., Ltd.. It received FDA 510(k) clearance on 2009-09-18 under 510(k) number K090742. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A?

DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A is a medical device that received FDA 510(k) clearance on 2009-09-18. The listed applicant is Samsung Mobile Display Co., Ltd.. The 510(k) number is K090742.

When did DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A receive FDA 510(k) clearance?

DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A received FDA 510(k) clearance on 2009-09-18, under 510(k) number K090742.

Who is the listed applicant for DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A?

The FDA 510(k) record lists Samsung Mobile Display Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A?

The FDA product code for DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A is MQB.

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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Other records listing Samsung Mobile Display Co., Ltd. as applicant

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.

K112751SDX-4343CSK112558DIGITAL FLAT PANEL X-RAY DETECTORK102321DIGITAL FLAT PANEL X-RAY DETECTOR MODEL SDX-4336CPK102587LLX240AB01

Related Devices (Code: MQB)

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.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, 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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