FDA 510(k)

Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)

K-번호: K231075 · 2023-06-20

결정일2023-06-20

제품 코드IZI

자문 위원회RA

결정Substantially Equivalent

기기 요약

Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss Meditec, Inc.. It received FDA 510(k) clearance on 2023-06-20 under 510(k) number K231075. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)?

Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) is a medical device that received FDA 510(k) clearance on 2023-06-20. The listed applicant is Carl Zeiss Meditec, Inc.. The 510(k) number is K231075.

When did Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) receive FDA 510(k) clearance?

Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) received FDA 510(k) clearance on 2023-06-20, under 510(k) number K231075.

Who is the listed applicant for Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)?

The FDA 510(k) record lists Carl Zeiss Meditec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)?

The FDA product code for Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) is IZI.

Carl Zeiss Meditec, Inc.를 신청인으로 등재한 기타 기록

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