FDA 510(k)

Advanced 牙科應用器

K 號：K172991 · 2018-07-10

決定日期2018-07-10

產品代碼LRK

諮詢委員會DE

決定相當於

器材摘要

Advanced Dental Applicance is the device name listed in this FDA 510(k) record. The listed applicant is Dasoft Partners. It received FDA 510(k) clearance on 2018-07-10 under 510(k) number K172991. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Advanced Dental Applicance?

Advanced Dental Applicance is a medical device that received FDA 510(k) clearance on 2018-07-10. The listed applicant is Dasoft Partners. The 510(k) number is K172991.

When did Advanced Dental Applicance receive FDA 510(k) clearance?

Advanced Dental Applicance received FDA 510(k) clearance on 2018-07-10, under 510(k) number K172991.

Who is the listed applicant for Advanced Dental Applicance?

The FDA 510(k) record lists Dasoft Partners as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Advanced Dental Applicance?

The FDA product code for Advanced Dental Applicance is LRK.

其他以 Dasoft Partners 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。

K203462Advanced 牙科器具

相關器械（代碼：LRK）

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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