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FDA 510(k)

荧光配件（黃色 560 及紅外線 800，並含 FLOW 800 選項）

K 號：K231075 · 2023-06-20

申請人Carl Zeiss Meditec, Inc.
決定日期2023-06-20
產品代碼IZI
諮詢委員會RA
決定相當於

器材摘要

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.

常見問題

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.

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相關器械（代碼：IZI）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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