FDA 510(k)

클리어패스 드isposable 인트루저

K-번호: K210251 · 2021-04-02

결정일2021-04-02

제품 코드GWG

자문 위원회NE (이 문서는 원문이 제공되지 않았기 때문에 번역할 수 없습니다. 원문을 제공해 주시면 번역을 도와드리겠습니다.)

결정Substantially Equivalent

기기 요약

ClearPath Disposable Introducer is the device name listed in this FDA 510(k) record. The listed applicant is Clearmind Biomedical. It received FDA 510(k) clearance on 2021-04-02 under 510(k) number K210251. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the ClearPath Disposable Introducer?

ClearPath Disposable Introducer is a medical device that received FDA 510(k) clearance on 2021-04-02. The listed applicant is Clearmind Biomedical. The 510(k) number is K210251.

When did ClearPath Disposable Introducer receive FDA 510(k) clearance?

ClearPath Disposable Introducer received FDA 510(k) clearance on 2021-04-02, under 510(k) number K210251.

Who is the listed applicant for ClearPath Disposable Introducer?

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

What is the FDA product code for ClearPath Disposable Introducer?

The FDA product code for ClearPath Disposable Introducer is GWG.

Clearmind Biomedical를 신청인으로 등재한 기타 기록

K230125뇌blade 시스템 K201308Axonpen, Axonmonitor, Axonbox, 태블릿

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