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FDA 510(k)

KONRAD, MODEL V.2.0

K-Number: K022307 · 2002-10-08

ApplicantMrc Systems GmbH
Decision Date2002-10-08
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KONRAD, MODEL V.2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Mrc Systems GmbH. It received FDA 510(k) clearance on 2002-10-08 under 510(k) number K022307. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KONRAD, MODEL V.2.0?

KONRAD, MODEL V.2.0 is a medical device that received FDA 510(k) clearance on 2002-10-08. The listed applicant is Mrc Systems GmbH. The 510(k) number is K022307.

When did KONRAD, MODEL V.2.0 receive FDA 510(k) clearance?

KONRAD, MODEL V.2.0 received FDA 510(k) clearance on 2002-10-08, under 510(k) number K022307.

Who is the listed applicant for KONRAD, MODEL V.2.0?

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

What is the FDA product code for KONRAD, MODEL V.2.0?

The FDA product code for KONRAD, MODEL V.2.0 is MUJ.

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 Mrc Systems GmbH 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.

K030609MODULEAFK011816MINI MULTILEAF COLLIMATOR, MODEL KMI

Related Devices (Code: MUJ)

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.

K260750Virtual Cone (1.0)Varian Medical Systems, Inc.K253050RadOncAIInformaiK260207Multimodality Simulation Workspace (MM Sim) (v1.0.0)Philips Medical Systems Nederland B.V.K252784eXaSkin PlusAnatomical Geometry S.L.K253078ART.1-USSeetreat Pty, Ltd.K252304syngo.via RT Image Suite VC10Varian Medical Systems, 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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