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FDA 510(k)

Lascod 印記材

K 號:K201184 · 2020-05-05

申請人Lascod Spa
決定日期2020-05-05
產品代碼ELW
諮詢委員會DE
決定相當於

器材摘要

Lascod Impression Materials is the device name listed in this FDA 510(k) record. The listed applicant is Lascod Spa. It received FDA 510(k) clearance on 2020-05-05 under 510(k) number K201184. 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 Lascod Impression Materials?

Lascod Impression Materials is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is Lascod Spa. The 510(k) number is K201184.

When did Lascod Impression Materials receive FDA 510(k) clearance?

Lascod Impression Materials received FDA 510(k) clearance on 2020-05-05, under 510(k) number K201184.

Who is the listed applicant for Lascod Impression Materials?

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

What is the FDA product code for Lascod Impression Materials?

The FDA product code for Lascod Impression Materials is ELW.

相關臨床試驗

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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。

官方來源

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