FDA 510(k)

Miro3D 點綴組織

K 號：K221520 · 2022-08-18

決定日期2022-08-18

產品代碼KGN

決定相當於

器材摘要

Miro3D Wound Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Reprise Biomedical, Inc.. It received FDA 510(k) clearance on 2022-08-18 under 510(k) number K221520. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常見問題

What is the Miro3D Wound Matrix?

Miro3D Wound Matrix is a medical device that received FDA 510(k) clearance on 2022-08-18. The listed applicant is Reprise Biomedical, Inc.. The 510(k) number is K221520.

When did Miro3D Wound Matrix receive FDA 510(k) clearance?

Miro3D Wound Matrix received FDA 510(k) clearance on 2022-08-18, under 510(k) number K221520.

Who is the listed applicant for Miro3D Wound Matrix?

The FDA 510(k) record lists Reprise Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Miro3D Wound Matrix?

The FDA product code for Miro3D Wound Matrix is KGN.

其他以 Reprise Biomedical, Inc. 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。

K240753Miro3D纖維傷口網絡 K240277MiroDry 準備材 K231614MiroTract 準創傷組織

相關器械（代碼：KGN）

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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