FDA 510(k)

SPIN-SWI

K 號：K173224 · 2018-02-23

決定日期2018-02-23

產品代碼LNH

諮詢委員會RA

決定相當於

器材摘要

SPIN-SWI is the device name listed in this FDA 510(k) record. The listed applicant is Spintech, Inc.. It received FDA 510(k) clearance on 2018-02-23 under 510(k) number K173224. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SPIN-SWI?

SPIN-SWI is a medical device that received FDA 510(k) clearance on 2018-02-23. The listed applicant is Spintech, Inc.. The 510(k) number is K173224.

When did SPIN-SWI receive FDA 510(k) clearance?

SPIN-SWI received FDA 510(k) clearance on 2018-02-23, under 510(k) number K173224.

Who is the listed applicant for SPIN-SWI?

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

What is the FDA product code for SPIN-SWI?

The FDA product code for SPIN-SWI is LNH.

其他以 Spintech, Inc. 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。

K223079階段 K210843階段

相關器械（代碼：LNH）

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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