FDA 510(k)

노블리언 장기주파수 알렉산드라이트 & Nd: YAG 레이저 시스템

K-번호: K182663 · 2018-11-30

결정일2018-11-30

제품 코드GEX

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

결정대체적으로 동일

기기 요약

Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Finemec Co., Ltd.. It received FDA 510(k) clearance on 2018-11-30 under 510(k) number K182663. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System?

Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System is a medical device that received FDA 510(k) clearance on 2018-11-30. The listed applicant is Finemec Co., Ltd.. The 510(k) number is K182663.

When did Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System receive FDA 510(k) clearance?

Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System received FDA 510(k) clearance on 2018-11-30, under 510(k) number K182663.

Who is the listed applicant for Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System?

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

What is the FDA product code for Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System?

The FDA product code for Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System is GEX. This falls under the Gastroenterology category.

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노블리언 장기주파수 알렉산드라이트 & Nd: YAG 레이저 시스템

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: GEX)

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