FDA 510(k)

라이트셀 데라이어; 라이트셀 데라이어 라이트; 라이트셀 듀엣; 라이트셀 인피니티

K-번호: K170179 · 2017-09-18

결정일2017-09-18

제품 코드GEX

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

결정대체적으로 동일

기기 요약

LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity is the device name listed in this FDA 510(k) record. The listed applicant is Lumenis, Ltd.. It received FDA 510(k) clearance on 2017-09-18 under 510(k) number K170179. 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 LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity?

LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity is a medical device that received FDA 510(k) clearance on 2017-09-18. The listed applicant is Lumenis, Ltd.. The 510(k) number is K170179.

When did LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity receive FDA 510(k) clearance?

LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity received FDA 510(k) clearance on 2017-09-18, under 510(k) number K170179.

Who is the listed applicant for LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity?

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

What is the FDA product code for LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity?

The FDA product code for LightSheer Desire; LightSheer Desire Light; LightSheer Duet; LightSheer Infinity is GEX. This falls under the Gastroenterology category.