FDA 510(k)

Arrow硬脊膜外針 KZ-05500-007(Luer)；KZ-05500-009 (NRFit)

K 號：K190026 · 2019-08-21

決定日期2019-08-21

產品代碼BSP

諮詢委員會AN

決定相當於

器材摘要

Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit) is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2019-08-21 under 510(k) number K190026. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit)?

Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit) is a medical device that received FDA 510(k) clearance on 2019-08-21. The listed applicant is Teleflex Medical. The 510(k) number is K190026.

When did Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit) receive FDA 510(k) clearance?

Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit) received FDA 510(k) clearance on 2019-08-21, under 510(k) number K190026.

Who is the listed applicant for Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit)?

FDA 510(k) 記錄將Teleflex Medical列為申請人。這並不單獨確立設備製造商的身份。

What is the FDA product code for Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit)?

The FDA product code for Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit) is BSP.

其他以 Teleflex Medical 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。

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相關器械（代碼：BSP）

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。

K243690SonoMSKPAJUNK GmbH Medizintechnologie K243682SonoPlex STIM；SonoPlex IIPAJUNK GmbH Medizintechnologie K250774SPROTTE® 标準 (LUER/NRFit®) 腰椎穿刺PAJUNK GmbH Medizintechnologie K243525SonoTAP 及 SonoTAP IIPAJUNK GmbH Medizintechnologie K241953SPROTTE®標準（LUER/NRFit®）麻醉學PAJUNK GmbH Medizintechnologie K241954SonoBlock；SonoBlock IIPAJUNK GmbH Medizintechnologie

官方來源

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資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。