FDA 510(k)

大盆地志贺毒素直接測試

K 號：K152955 · 2016-03-22

決定日期2016-03-22

產品代碼PCH

諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)

決定相當於

器材摘要

Great Basin Shiga Toxin Direct Test is the device name listed in this FDA 510(k) record. The listed applicant is Great Basin Scientific, Inc.. It received FDA 510(k) clearance on 2016-03-22 under 510(k) number K152955. The device is classified under product code PCH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Great Basin Shiga Toxin Direct Test?

Great Basin Shiga Toxin Direct Test is a medical device that received FDA 510(k) clearance on 2016-03-22. The listed applicant is Great Basin Scientific, Inc.. The 510(k) number is K152955.

When did Great Basin Shiga Toxin Direct Test receive FDA 510(k) clearance?

Great Basin Shiga Toxin Direct Test received FDA 510(k) clearance on 2016-03-22, under 510(k) number K152955.

Who is the listed applicant for Great Basin Shiga Toxin Direct Test?

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

What is the FDA product code for Great Basin Shiga Toxin Direct Test?

The FDA product code for Great Basin Shiga Toxin Direct Test is PCH.

其他以 Great Basin Scientific, 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。

K163571大盆地糞便細菌病原體檢測組合 K170284Great Basin Bordetella直接測試 K152470大盆地葡萄球菌ID/R血液培養組合

相關器械（代碼：PCH）

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。

K253722LIAISON PLEX 消化道柔軟性試驗Luminex Corporation K254032QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini BQIAGEN GmbH K251721Xpert GI PanelCepheid K252329QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini BQIAGEN GmbH K251868山貓融合胃腸細菌試驗Hologic K251993山貓融合內分泌系統廣範細菌試驗Hologic, Inc.

官方來源

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