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FDA 510(k)

Corvus Radiation Therapy Planning System

K-Number: K211034 · 2021-05-06

ApplicantBest Nomos
Decision Date2021-05-06
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Corvus Radiation Therapy Planning System is a medical device manufactured by Best Nomos. It received FDA 510(k) clearance on 2021-05-06 under approval number K211034. 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 Corvus Radiation Therapy Planning System?

Corvus Radiation Therapy Planning System is a medical device that received FDA 510(k) clearance on 2021-05-06. It is manufactured by Best Nomos. The 510(k) number is K211034.

When was Corvus Radiation Therapy Planning System approved by the FDA?

Corvus Radiation Therapy Planning System received FDA 510(k) clearance on 2021-05-06, under approval number K211034.

What company makes Corvus Radiation Therapy Planning System?

Corvus Radiation Therapy Planning System is manufactured by Best Nomos.

What is the FDA product code for Corvus Radiation Therapy Planning System?

The FDA product code for Corvus Radiation Therapy Planning System is MUJ.

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Related PubMed Literature

PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026) PMID: 41887630 Capacity building for ethical use of artificial intelligence in health: protocol for a scoping review of training initiatives and gaps in Africa. BMJ open (2026) PMID: 41596046 A Review of 3D-Printed Medical Devices for Cancer Radiation Therapy. Bioengineering (Basel, Switzerland) (2026) PMID: 41052472 Successful management of recurrent multiple intracerebral TFE3-rearranged epithelioid hemangioendothelioma with repeated intervention and active surveillance: illustrative case. Journal of neurosurgery. Case lessons (2025)

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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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