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FDA 510(k)

Sildent 快速輕體，Sildent 快速重體，Sildent 咬合

K 號：K181604 · 2018-11-28

申請人Hrs Co., Ltd.
決定日期2018-11-28
產品代碼ELW
諮詢委員會DE
決定相當於

器材摘要

Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite is the device name listed in this FDA 510(k) record. The listed applicant is Hrs Co., Ltd.. It received FDA 510(k) clearance on 2018-11-28 under 510(k) number K181604. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite?

Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite is a medical device that received FDA 510(k) clearance on 2018-11-28. The listed applicant is Hrs Co., Ltd.. The 510(k) number is K181604.

When did Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite receive FDA 510(k) clearance?

Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite received FDA 510(k) clearance on 2018-11-28, under 510(k) number K181604.

Who is the listed applicant for Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite?

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

What is the FDA product code for Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite?

The FDA product code for Sildent Fast Light Body, Sildent Fast Heavy Body, Sildent Bite is ELW.

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相關器械（代碼：ELW）

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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