FDA 510(k)

Racz Neurostat RF Generator

K-번호: K232632 · 2024-05-24

결정일2024-05-24

제품 코드GXD

자문 위원회NE (이 문서는 원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.)

결정Substantially Equivalent

기기 요약

Racz Neurostat RF Generator is the device name listed in this FDA 510(k) record. The listed applicant is Epimed International. It received FDA 510(k) clearance on 2024-05-24 under 510(k) number K232632. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Racz Neurostat RF Generator?

Racz Neurostat RF Generator is a medical device that received FDA 510(k) clearance on 2024-05-24. The listed applicant is Epimed International. The 510(k) number is K232632.

When did Racz Neurostat RF Generator receive FDA 510(k) clearance?

Racz Neurostat RF Generator received FDA 510(k) clearance on 2024-05-24, under 510(k) number K232632.

Who is the listed applicant for Racz Neurostat RF Generator?

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

What is the FDA product code for Racz Neurostat RF Generator?

The FDA product code for Racz Neurostat RF Generator is GXD.

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Racz Neurostat RF Generator

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: GXD)

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