FDA 510(k)

牙科手持機，型號CA160、CA160L及CA500L

K 號：K220577 · 2022-07-29

決定日期2022-07-29

產品代碼EGS

諮詢委員會DE

決定相當於

器材摘要

Dental Handpiece, Model CA160, CA160L, and CA500L is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Nx Co., Ltd.. It received FDA 510(k) clearance on 2022-07-29 under 510(k) number K220577. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Dental Handpiece, Model CA160, CA160L, and CA500L?

Dental Handpiece, Model CA160, CA160L, and CA500L is a medical device that received FDA 510(k) clearance on 2022-07-29. The listed applicant is Micro-Nx Co., Ltd.. The 510(k) number is K220577.

When did Dental Handpiece, Model CA160, CA160L, and CA500L receive FDA 510(k) clearance?

Dental Handpiece, Model CA160, CA160L, and CA500L received FDA 510(k) clearance on 2022-07-29, under 510(k) number K220577.

Who is the listed applicant for Dental Handpiece, Model CA160, CA160L, and CA500L?

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

What is the FDA product code for Dental Handpiece, Model CA160, CA160L, and CA500L?

The FDA product code for Dental Handpiece, Model CA160, CA160L, and CA500L is EGS.

其他以 Micro-Nx 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。

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相關器械（代碼：EGS）

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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