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FDA 510(k)

GR17 DIGITAL DETECTOR

K-Number: K052136 · 2005-08-25

ApplicantAnrad Corp.
Decision Date2005-08-25
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GR17 DIGITAL DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Anrad Corp.. It received FDA 510(k) clearance on 2005-08-25 under 510(k) number K052136. 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 GR17 DIGITAL DETECTOR?

GR17 DIGITAL DETECTOR is a medical device that received FDA 510(k) clearance on 2005-08-25. The listed applicant is Anrad Corp.. The 510(k) number is K052136.

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

GR17 DIGITAL DETECTOR received FDA 510(k) clearance on 2005-08-25, under 510(k) number K052136.

Who is the listed applicant for GR17 DIGITAL DETECTOR?

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 GR17 DIGITAL DETECTOR?

The FDA product code for GR17 DIGITAL DETECTOR 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K042821DIGITAL DETECTOR, MODEL GR17

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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