IMD 的腰椎穿刺針
K 號：K170112 · 2018-02-02
廣告
器材摘要
IMD's Lumbar Puncture Needle is the device name listed in this FDA 510(k) record. The listed applicant is International Medical Development, Inc.(Imd). It received FDA 510(k) clearance on 2018-02-02 under 510(k) number K170112. 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 IMD's Lumbar Puncture Needle?
IMD's Lumbar Puncture Needle is a medical device that received FDA 510(k) clearance on 2018-02-02. The listed applicant is International Medical Development, Inc.(Imd). The 510(k) number is K170112.
When did IMD's Lumbar Puncture Needle receive FDA 510(k) clearance?
IMD's Lumbar Puncture Needle received FDA 510(k) clearance on 2018-02-02, under 510(k) number K170112.
Who is the listed applicant for IMD's Lumbar Puncture Needle?
The FDA 510(k) record lists International Medical Development, Inc.(Imd) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMD's Lumbar Puncture Needle?
The FDA product code for IMD's Lumbar Puncture Needle is BSP.
相關臨床試驗
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。
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 MedizintechnologieK243682SonoPlex STIM；SonoPlex IIPAJUNK GmbH MedizintechnologieK250774SPROTTE® 标準 (LUER/NRFit®) 腰椎穿刺PAJUNK GmbH MedizintechnologieK243525SonoTAP 及 SonoTAP IIPAJUNK GmbH MedizintechnologieK241953SPROTTE®標準（LUER/NRFit®）麻醉學PAJUNK GmbH MedizintechnologieK241954SonoBlock；SonoBlock IIPAJUNK GmbH Medizintechnologie
官方來源
在 FDA 資料庫中查看 →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。
廣告