FDA 510(k)

Vascette HP（止血墊）

K 號：K220566 · 2022-07-29

決定日期2022-07-29

產品代碼QSY

決定相當於

器材摘要

Vascette HP (hemostatic pad) is the device name listed in this FDA 510(k) record. The listed applicant is Koag, LLC. It received FDA 510(k) clearance on 2022-07-29 under 510(k) number K220566. The device is classified under product code QSY. FDA Decision: Substantially Equivalent.

常見問題

What is the Vascette HP (hemostatic pad)?

Vascette HP (hemostatic pad) is a medical device that received FDA 510(k) clearance on 2022-07-29. The listed applicant is Koag, LLC. The 510(k) number is K220566.

When did Vascette HP (hemostatic pad) receive FDA 510(k) clearance?

Vascette HP (hemostatic pad) received FDA 510(k) clearance on 2022-07-29, under 510(k) number K220566.

Who is the listed applicant for Vascette HP (hemostatic pad)?

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

What is the FDA product code for Vascette HP (hemostatic pad)?

The FDA product code for Vascette HP (hemostatic pad) is QSY.

相關器械（代碼：QSY）

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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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：QSY）

官方來源