FDA 510(k)

다기능 플랫폼 시스템 (BL-M10)

K-번호: K240474 · 2024-05-20

신청자Shanghai Bele Medical Technology Co.,Ltd

결정일2024-05-20

제품 코드GEX

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

결정대체적으로 동일

기기 요약

Multi-function Platform Systems (BL-M10) is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Bele Medical Technology Co.,Ltd. It received FDA 510(k) clearance on 2024-05-20 under 510(k) number K240474. 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 Multi-function Platform Systems (BL-M10)?

Multi-function Platform Systems (BL-M10) is a medical device that received FDA 510(k) clearance on 2024-05-20. The listed applicant is Shanghai Bele Medical Technology Co.,Ltd. The 510(k) number is K240474.

When did Multi-function Platform Systems (BL-M10) receive FDA 510(k) clearance?

Multi-function Platform Systems (BL-M10) received FDA 510(k) clearance on 2024-05-20, under 510(k) number K240474.

Who is the listed applicant for Multi-function Platform Systems (BL-M10)?

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

What is the FDA product code for Multi-function Platform Systems (BL-M10)?

The FDA product code for Multi-function Platform Systems (BL-M10) is GEX. This falls under the Gastroenterology category.

Shanghai Bele Medical Technology Co.,Ltd를 신청인으로 등재한 기타 기록

K240386피코초 Nd:YAG 레이저 시스템 (BL-C10)K231131다이오드 레이저 본드 셀렉션 시스템

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