FDA 510(k)

Medispine - 頸椎針，Glospine - 頸椎針

K 號：K212982 · 2022-07-29

決定日期2022-07-29

產品代碼BSP

諮詢委員會AN

決定相當於

器材摘要

Medispine - Spinal Needle, Glospine - Spinal Needle is the device name listed in this FDA 510(k) record. The listed applicant is Global Medikit Limited. It received FDA 510(k) clearance on 2022-07-29 under 510(k) number K212982. 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 Medispine - Spinal Needle, Glospine - Spinal Needle?

Medispine - Spinal Needle, Glospine - Spinal Needle is a medical device that received FDA 510(k) clearance on 2022-07-29. The listed applicant is Global Medikit Limited. The 510(k) number is K212982.

When did Medispine - Spinal Needle, Glospine - Spinal Needle receive FDA 510(k) clearance?

Medispine - Spinal Needle, Glospine - Spinal Needle received FDA 510(k) clearance on 2022-07-29, under 510(k) number K212982.

Who is the listed applicant for Medispine - Spinal Needle, Glospine - Spinal Needle?

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

What is the FDA product code for Medispine - Spinal Needle, Glospine - Spinal Needle?

The FDA product code for Medispine - Spinal Needle, Glospine - Spinal Needle is BSP.

其他以 Global Medikit Limited 為申請人之記錄

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K193158ACENT® 頸內靜脈針

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。

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官方來源

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