FDA 510(k)

RAYSkan a-Expert

K 號：K232325 · 2024-04-18

決定日期2024-04-18

產品代碼MUH

諮詢委員會DE

決定相當於

器材摘要

RAYSCAN a-Expert is the device name listed in this FDA 510(k) record. The listed applicant is Ray Co., Ltd.. It received FDA 510(k) clearance on 2024-04-18 under 510(k) number K232325. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the RAYSCAN a-Expert?

RAYSCAN a-Expert is a medical device that received FDA 510(k) clearance on 2024-04-18. The listed applicant is Ray Co., Ltd.. The 510(k) number is K232325.

When did RAYSCAN a-Expert receive FDA 510(k) clearance?

RAYSCAN a-Expert received FDA 510(k) clearance on 2024-04-18, under 510(k) number K232325.

Who is the listed applicant for RAYSCAN a-Expert?

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

What is the FDA product code for RAYSCAN a-Expert?

The FDA product code for RAYSCAN a-Expert is MUH.

其他以 Ray Co., Ltd. 為申請人之記錄

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。

K260462RCT800 K251798RCT700 K251109SMARTDent K243903RCT600 K233625瑞德恩 SW K232287RAYSCAN a-Expert3D

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相關器械（代碼：MUH）

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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官方來源

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