FDA 510(k)

다이어프램 푸즈 MultiPulse HoPLUS

K-번호: K161257 · 2017-03-31

결정일2017-03-31

제품 코드GEX

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

결정대체적으로 동일

기기 요약

MultiPulse HoPLUS is the device name listed in this FDA 510(k) record. The listed applicant is Asclepion Laser Technologies GmbH. It received FDA 510(k) clearance on 2017-03-31 under 510(k) number K161257. 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 MultiPulse HoPLUS?

MultiPulse HoPLUS is a medical device that received FDA 510(k) clearance on 2017-03-31. The listed applicant is Asclepion Laser Technologies GmbH. The 510(k) number is K161257.

When did MultiPulse HoPLUS receive FDA 510(k) clearance?

MultiPulse HoPLUS received FDA 510(k) clearance on 2017-03-31, under 510(k) number K161257.

Who is the listed applicant for MultiPulse HoPLUS?

The FDA 510(k) record lists Asclepion Laser Technologies GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MultiPulse HoPLUS?

The FDA product code for MultiPulse HoPLUS is GEX. This falls under the Gastroenterology category.

Asclepion Laser Technologies GmbH를 신청인으로 등재한 기타 기록

K261094YellowStar K253100다이어프램 풀스 트랜스퍼트 퍼퓨저 K240831다이어트 솔로 K241600디어마블트 K240816미디오스타 K231876다이어프램 푸즈 MultiPulse HoPLUS

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