FDA 510(k)

Ziehm Vision RFD

K-번호: K240099 · 2024-02-05

결정일2024-02-05

제품 코드OWB

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

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기기 요약

Ziehm Vision RFD is the device name listed in this FDA 510(k) record. The listed applicant is Ziehm Imaging GmbH. It received FDA 510(k) clearance on 2024-02-05 under 510(k) number K240099. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Ziehm Vision RFD?

Ziehm Vision RFD is a medical device that received FDA 510(k) clearance on 2024-02-05. The listed applicant is Ziehm Imaging GmbH. The 510(k) number is K240099.

When did Ziehm Vision RFD receive FDA 510(k) clearance?

Ziehm Vision RFD received FDA 510(k) clearance on 2024-02-05, under 510(k) number K240099.

Who is the listed applicant for Ziehm Vision RFD?

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

What is the FDA product code for Ziehm Vision RFD?

The FDA product code for Ziehm Vision RFD is OWB.

Ziehm Imaging GmbH를 신청인으로 등재한 기타 기록

K243646Ziehm Solo FD K243735Ziehm Vision FD K243303Ziehm Vision RFD 3D K243328Ziehm Vision RFD K240020Ziehm Vision FD K234109Ziehm Solo FD

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