FDA 510(k)

巴德柔 mesh；巴德柔柔 mesh 預成型

K 號：K250098 · 2025-04-09

決定日期2025-04-09

產品代碼FTL

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

Bard Soft Mesh; Bard Soft Mesh Pre-Shaped is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 2025-04-09 under 510(k) number K250098. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bard Soft Mesh; Bard Soft Mesh Pre-Shaped?

Bard Soft Mesh; Bard Soft Mesh Pre-Shaped is a medical device that received FDA 510(k) clearance on 2025-04-09. The listed applicant is Davol, Inc.. The 510(k) number is K250098.

When did Bard Soft Mesh; Bard Soft Mesh Pre-Shaped receive FDA 510(k) clearance?

Bard Soft Mesh; Bard Soft Mesh Pre-Shaped received FDA 510(k) clearance on 2025-04-09, under 510(k) number K250098.

Who is the listed applicant for Bard Soft Mesh; Bard Soft Mesh Pre-Shaped?

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

What is the FDA product code for Bard Soft Mesh; Bard Soft Mesh Pre-Shaped?

The FDA product code for Bard Soft Mesh; Bard Soft Mesh Pre-Shaped is FTL.

其他以 Davol, 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。

K251557巴德® 網膜；巴德® 預成型網膜

相關器械（代碼：FTL）

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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