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FDA 510(k)

Zirdent 齒科澱粉礦石空白板 & 齒科澱粉礦石預著色空白板

K 號:K212259 · 2021-11-12

決定日期2021-11-12
產品代碼EIH
諮詢委員會DE
決定相當於

器材摘要

Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank is the device name listed in this FDA 510(k) record. The listed applicant is Zirdent New Material Co., Ltd.. It received FDA 510(k) clearance on 2021-11-12 under 510(k) number K212259. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank?

Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank is a medical device that received FDA 510(k) clearance on 2021-11-12. The listed applicant is Zirdent New Material Co., Ltd.. The 510(k) number is K212259.

When did Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank receive FDA 510(k) clearance?

Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank received FDA 510(k) clearance on 2021-11-12, under 510(k) number K212259.

Who is the listed applicant for Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank?

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

What is the FDA product code for Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank?

The FDA product code for Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank is EIH.

相關臨床試驗

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相關器械(代碼:EIH)

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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