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FDA 510(k)

W&H 協助儀雙用

K 號:K171553 · 2017-12-08

決定日期2017-12-08
產品代碼EFB
諮詢委員會DE
決定相當於

器材摘要

W&H Assistina Twin is the device name listed in this FDA 510(k) record. The listed applicant is W&H Dentalwerk Buermoos GmbH. It received FDA 510(k) clearance on 2017-12-08 under 510(k) number K171553. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the W&H Assistina Twin?

W&H Assistina Twin is a medical device that received FDA 510(k) clearance on 2017-12-08. The listed applicant is W&H Dentalwerk Buermoos GmbH. The 510(k) number is K171553.

When did W&H Assistina Twin receive FDA 510(k) clearance?

W&H Assistina Twin received FDA 510(k) clearance on 2017-12-08, under 510(k) number K171553.

Who is the listed applicant for W&H Assistina Twin?

The FDA 510(k) record lists W&H Dentalwerk Buermoos GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for W&H Assistina Twin?

The FDA product code for W&H Assistina Twin is EFB.

相關臨床試驗

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其他以 W&H Dentalwerk Buermoos GmbH 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。

相關器械(代碼:EFB)

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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