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FDA 510(k)

單次使用針筒 NM600/610

K 號:K153625 · 2016-02-12

決定日期2016-02-12
產品代碼FBK
諮詢委員會GU
決定相當於

器材摘要

Single Use Injector NM600/610 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K153625. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Single Use Injector NM600/610?

Single Use Injector NM600/610 is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K153625.

When did Single Use Injector NM600/610 receive FDA 510(k) clearance?

Single Use Injector NM600/610 received FDA 510(k) clearance on 2016-02-12, under 510(k) number K153625.

Who is the listed applicant for Single Use Injector NM600/610?

FDA 510(k) 記錄將Olympus Medical Systems Corp. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Single Use Injector NM600/610?

The FDA product code for Single Use Injector NM600/610 is FBK.

相關臨床試驗

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其他以 Olympus Medical Systems Corp. 為申請人之記錄

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相關器械(代碼:FBK)

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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