Corvus Radiation Therapy Planning System— 510(k) K211034

Name: FDA 510(k) clearance K211034
Creator: U.S. Food and Drug Administration
Published: 2021-05-06

Substantially Equivalent

Best Nomos

FDA 510(k) clearance K211034 for Corvus Radiation Therapy Planning System, Substantially Equivalent on 2021-05-06. Applicant: Best Nomos. Device class: 2.

Clearance details

Applicant: Best Nomos
Product code: Code MUJ
Device class: Class 2
Regulation: 21 CFR 892.5050
Advisory panel: Radiology
Date received: 2021-04-07
Decision date: 2021-05-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Pittsburgh, PA, US

Download summary PDF View on FDA.gov ↗

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K201350 — CORVUS2020-09-20
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K100092 — CORVUS RADIATION THERAPY PLANNING SYSTEM2010-02-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.