免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

呼吸識別 Hp 实验室系統

K 號:K162150 · 2016-10-31

決定日期2016-10-31
產品代碼MSQ
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

BreathID Hp Lab System is the device name listed in this FDA 510(k) record. The listed applicant is Exalenz Bioscience , Ltd.. It received FDA 510(k) clearance on 2016-10-31 under 510(k) number K162150. The device is classified under product code MSQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BreathID Hp Lab System?

BreathID Hp Lab System is a medical device that received FDA 510(k) clearance on 2016-10-31. The listed applicant is Exalenz Bioscience , Ltd.. The 510(k) number is K162150.

When did BreathID Hp Lab System receive FDA 510(k) clearance?

BreathID Hp Lab System received FDA 510(k) clearance on 2016-10-31, under 510(k) number K162150.

Who is the listed applicant for BreathID Hp Lab System?

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

What is the FDA product code for BreathID Hp Lab System?

The FDA product code for BreathID Hp Lab System is MSQ.

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。

其他以 Exalenz Bioscience , Ltd. 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。

相關器械(代碼:MSQ)

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

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。

↑