FDA 510(k)

吸引針 (2189)

K 號：K241874 · 2024-09-24

決定日期2024-09-24

產品代碼OCX

諮詢委員會GU

決定相當於

器材摘要

Aspiration Catheter (2189) is the device name listed in this FDA 510(k) record. The listed applicant is Hobbs Medical, Inc.. It received FDA 510(k) clearance on 2024-09-24 under 510(k) number K241874. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Aspiration Catheter (2189)?

Aspiration Catheter (2189) is a medical device that received FDA 510(k) clearance on 2024-09-24. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K241874.

When did Aspiration Catheter (2189) receive FDA 510(k) clearance?

Aspiration Catheter (2189) received FDA 510(k) clearance on 2024-09-24, under 510(k) number K241874.

Who is the listed applicant for Aspiration Catheter (2189)?

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

What is the FDA product code for Aspiration Catheter (2189)?

The FDA product code for Aspiration Catheter (2189) is OCX.

其他以 Hobbs Medical, Inc. 為申請人之記錄

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K182927肺細胞刷

相關器械（代碼：OCX）

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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