FDA 510(k)

코루스 방사선 치료 계획 시스템

K-번호: K211034 · 2021-05-06

결정일2021-05-06

제품 코드MUJ

자문 위원회[원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.]

결정대체적으로 동일

기기 요약

Corvus Radiation Therapy Planning System is the device name listed in this FDA 510(k) record. The listed applicant is Best Nomos. It received FDA 510(k) clearance on 2021-05-06 under 510(k) number K211034. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

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. The listed applicant is Best Nomos. The 510(k) number is K211034.

When did Corvus Radiation Therapy Planning System receive FDA 510(k) clearance?

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

Who is the listed applicant for Corvus Radiation Therapy Planning System?

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 Radiation Therapy Planning System?

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

Best Nomos를 신청인으로 등재한 기타 기록

K201350코르베스 K170345소프트디소

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