FDA 510(k)

CORVUS

K-Number: K201350 · 2020-09-20

Decision Date2020-09-20

Product CodeMUJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CORVUS is the device name listed in this FDA 510(k) record. The listed applicant is Best Nomos. It received FDA 510(k) clearance on 2020-09-20 under 510(k) 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. The listed applicant is Best Nomos. The 510(k) number is K201350.

When did CORVUS receive FDA 510(k) clearance?

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

Who is the listed applicant for CORVUS?

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

What is the FDA product code for CORVUS?

The FDA product code for CORVUS is MUJ.

Other records listing Best Nomos 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.

K211034Corvus Radiation Therapy Planning System K170345SOFTDISO

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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.