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FDA 510(k)

呼吸粉紅系列搭配DentiTrac

K 號:K170692 · 2017-05-26

決定日期2017-05-26
產品代碼LRK
諮詢委員會DE
決定相當於

器材摘要

Respire Pink Series with DentiTrac is the device name listed in this FDA 510(k) record. The listed applicant is Respire Medical Holding. It received FDA 510(k) clearance on 2017-05-26 under 510(k) number K170692. 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 Respire Pink Series with DentiTrac?

Respire Pink Series with DentiTrac is a medical device that received FDA 510(k) clearance on 2017-05-26. The listed applicant is Respire Medical Holding. The 510(k) number is K170692.

When did Respire Pink Series with DentiTrac receive FDA 510(k) clearance?

Respire Pink Series with DentiTrac received FDA 510(k) clearance on 2017-05-26, under 510(k) number K170692.

Who is the listed applicant for Respire Pink Series with DentiTrac?

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

What is the FDA product code for Respire Pink Series with DentiTrac?

The FDA product code for Respire Pink Series with DentiTrac is LRK.

相關臨床試驗

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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。

官方來源

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