FDA 510(k)

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K-번호: K210567 · 2022-09-30

결정일2022-09-30

제품 코드LFL

결정대체적으로 동일

기기 요약

Ultrasonic Surgical System is the device name listed in this FDA 510(k) record. The listed applicant is Miconvey Technologies Co., Ltd.. It received FDA 510(k) clearance on 2022-09-30 under 510(k) number K210567. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Ultrasonic Surgical System?

Ultrasonic Surgical System is a medical device that received FDA 510(k) clearance on 2022-09-30. The listed applicant is Miconvey Technologies Co., Ltd.. The 510(k) number is K210567.

When did Ultrasonic Surgical System receive FDA 510(k) clearance?

Ultrasonic Surgical System received FDA 510(k) clearance on 2022-09-30, under 510(k) number K210567.

Who is the listed applicant for Ultrasonic Surgical System?

The FDA 510(k) record lists Miconvey Technologies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ultrasonic Surgical System?

The FDA product code for Ultrasonic Surgical System is LFL.

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기기 요약

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관련 임상시험

관련 기기 (코드: LFL)

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