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FDA 510(k)

IMICRYL 印模材質

K 號：K213890 · 2022-02-11

申請人Imicryl Dis Malzemeleri San. VE Tic. A.S.
決定日期2022-02-11
產品代碼ELW
諮詢委員會DE
決定相當於

器材摘要

IMICRYL Impression Materials is the device name listed in this FDA 510(k) record. The listed applicant is Imicryl Dis Malzemeleri San. VE Tic. A.S.. It received FDA 510(k) clearance on 2022-02-11 under 510(k) number K213890. 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 IMICRYL Impression Materials?

IMICRYL Impression Materials is a medical device that received FDA 510(k) clearance on 2022-02-11. The listed applicant is Imicryl Dis Malzemeleri San. VE Tic. A.S.. The 510(k) number is K213890.

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

IMICRYL Impression Materials received FDA 510(k) clearance on 2022-02-11, under 510(k) number K213890.

Who is the listed applicant for IMICRYL Impression Materials?

The FDA 510(k) record lists Imicryl Dis Malzemeleri San. VE Tic. A.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMICRYL Impression Materials?

The FDA product code for IMICRYL 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。

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官方來源

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