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FDA 510(k)

NPseal (20及25)

K 號:K241522 · 2024-08-15

決定日期2024-08-15
產品代碼OKO
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

NPseal (20 and 25) is the device name listed in this FDA 510(k) record. The listed applicant is Guard Medical, Inc.. It received FDA 510(k) clearance on 2024-08-15 under 510(k) number K241522. The device is classified under product code OKO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NPseal (20 and 25)?

NPseal (20 and 25) is a medical device that received FDA 510(k) clearance on 2024-08-15. The listed applicant is Guard Medical, Inc.. The 510(k) number is K241522.

When did NPseal (20 and 25) receive FDA 510(k) clearance?

NPseal (20 and 25) received FDA 510(k) clearance on 2024-08-15, under 510(k) number K241522.

Who is the listed applicant for NPseal (20 and 25)?

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

What is the FDA product code for NPseal (20 and 25)?

The FDA product code for NPseal (20 and 25) is OKO.

相關臨床試驗

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其他以 Guard Medical, Inc. 為申請人之記錄

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相關器械(代碼:OKO)

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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