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FDA 510(k)

DIGITAL DETECTOR, MODEL GR17

K-Number: K042821 · 2004-10-22

ApplicantAnrad Corp.
Decision Date2004-10-22
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL DETECTOR, MODEL GR17 is the device name listed in this FDA 510(k) record. The listed applicant is Anrad Corp.. It received FDA 510(k) clearance on 2004-10-22 under 510(k) number K042821. 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 DETECTOR, MODEL GR17?

DIGITAL DETECTOR, MODEL GR17 is a medical device that received FDA 510(k) clearance on 2004-10-22. The listed applicant is Anrad Corp.. The 510(k) number is K042821.

When did DIGITAL DETECTOR, MODEL GR17 receive FDA 510(k) clearance?

DIGITAL DETECTOR, MODEL GR17 received FDA 510(k) clearance on 2004-10-22, under 510(k) number K042821.

Who is the listed applicant for DIGITAL DETECTOR, MODEL GR17?

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

What is the FDA product code for DIGITAL DETECTOR, MODEL GR17?

The FDA product code for DIGITAL DETECTOR, MODEL GR17 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 Anrad Corp. 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.

K052136GR17 DIGITAL DETECTOR

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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