FDA 510(k)

HF Surgery Generator 400KHZ

K-번호: K230194 · 2023-03-22

신청자Richard Wolf Medical Instruments Corporation

결정일2023-03-22

제품 코드GEI

자문 위원회SU

결정Substantially Equivalent

기기 요약

HF Surgery Generator 400KHZ is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corporation. It received FDA 510(k) clearance on 2023-03-22 under 510(k) number K230194. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the HF Surgery Generator 400KHZ?

HF Surgery Generator 400KHZ is a medical device that received FDA 510(k) clearance on 2023-03-22. The listed applicant is Richard Wolf Medical Instruments Corporation. The 510(k) number is K230194.

When did HF Surgery Generator 400KHZ receive FDA 510(k) clearance?

HF Surgery Generator 400KHZ received FDA 510(k) clearance on 2023-03-22, under 510(k) number K230194.

Who is the listed applicant for HF Surgery Generator 400KHZ?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HF Surgery Generator 400KHZ?

The FDA product code for HF Surgery Generator 400KHZ is GEI.

Richard Wolf Medical Instruments Corporation를 신청인으로 등재한 기타 기록

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