FDA 510(k)

CORVUS

K-Number: K201350 · 2020-09-20

Decision Date2020-09-20

Product CodeMUJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CORVUS is a medical device manufactured by Best Nomos. It received FDA 510(k) clearance on 2020-09-20 under approval number K201350. 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?

CORVUS is a medical device that received FDA 510(k) clearance on 2020-09-20. It is manufactured by Best Nomos. The 510(k) number is K201350.

When was CORVUS approved by the FDA?

CORVUS received FDA 510(k) clearance on 2020-09-20, under approval number K201350.

What company makes CORVUS?

CORVUS is manufactured by Best Nomos.

What is the FDA product code for CORVUS?

The FDA product code for CORVUS is MUJ.

Other Devices by Best Nomos

K170345SOFTDISO K211034Corvus Radiation Therapy Planning System

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.