FDA 510(k)

目標可拆式線圈

K 號：K242243 · 2024-08-29

決定日期2024-08-29

產品代碼HCG

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

Target Detachable Coils is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Neurovscular. It received FDA 510(k) clearance on 2024-08-29 under 510(k) number K242243. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Target Detachable Coils?

Target Detachable Coils is a medical device that received FDA 510(k) clearance on 2024-08-29. The listed applicant is Stryker Neurovscular. The 510(k) number is K242243.

When did Target Detachable Coils receive FDA 510(k) clearance?

Target Detachable Coils received FDA 510(k) clearance on 2024-08-29, under 510(k) number K242243.

Who is the listed applicant for Target Detachable Coils?

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

What is the FDA product code for Target Detachable Coils?

The FDA product code for Target Detachable Coils is HCG.

其他以 Stryker Neurovscular 為申請人之記錄

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K261772目標Xtra可拆式線圈

相關器械（代碼：HCG）

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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