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FDA 510(k)

羅斯因膠原粉

K 號:K254034 · 2026-06-03

決定日期2026-06-03
產品代碼KGN
決定相當於

器材摘要

Roosin Collagen Powder is the device name listed in this FDA 510(k) record. The listed applicant is Roosin Medical Co., Ltd.. It received FDA 510(k) clearance on 2026-06-03 under 510(k) number K254034. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常見問題

What is the Roosin Collagen Powder?

Roosin Collagen Powder is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Roosin Medical Co., Ltd.. The 510(k) number is K254034.

When did Roosin Collagen Powder receive FDA 510(k) clearance?

Roosin Collagen Powder received FDA 510(k) clearance on 2026-06-03, under 510(k) number K254034.

Who is the listed applicant for Roosin Collagen Powder?

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

What is the FDA product code for Roosin Collagen Powder?

The FDA product code for Roosin Collagen Powder is KGN.

相關臨床試驗

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其他以 Roosin Medical Co., Ltd. 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。

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。

官方來源

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