FDA 510(k)

Primo牙科雷射（Primo、Primo Komfort、Primo Lite、Primo Blue 及 Primo Triplo）

K 號：K232222 · 2023-11-27

決定日期2023-11-27

產品代碼NVK

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo) is the device name listed in this FDA 510(k) record. The listed applicant is Medency S.R.L.. It received FDA 510(k) clearance on 2023-11-27 under 510(k) number K232222. The device is classified under product code NVK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo)?

Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo) is a medical device that received FDA 510(k) clearance on 2023-11-27. The listed applicant is Medency S.R.L.. The 510(k) number is K232222.

When did Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo) receive FDA 510(k) clearance?

Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo) received FDA 510(k) clearance on 2023-11-27, under 510(k) number K232222.

Who is the listed applicant for Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo)?

The FDA 510(k) record lists Medency S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo)?

The FDA product code for Primo Dental Laser (Primo, Primo Komfort, Primo Lite, Primo Blue, and Primo Triplo) is NVK.

其他以 Medency S.R.L. 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：NVK）

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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