爵士獨奏感測器
K 號:K163224 · 2017-03-09
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器材摘要
JAZZ SOLO Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Jazz Imaging, LLC. It received FDA 510(k) clearance on 2017-03-09 under 510(k) number K163224. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the JAZZ SOLO Sensor?
JAZZ SOLO Sensor is a medical device that received FDA 510(k) clearance on 2017-03-09. The listed applicant is Jazz Imaging, LLC. The 510(k) number is K163224.
When did JAZZ SOLO Sensor receive FDA 510(k) clearance?
JAZZ SOLO Sensor received FDA 510(k) clearance on 2017-03-09, under 510(k) number K163224.
Who is the listed applicant for JAZZ SOLO Sensor?
The FDA 510(k) record lists Jazz Imaging, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JAZZ SOLO Sensor?
The FDA product code for JAZZ SOLO Sensor is MUH.
相關臨床試驗
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相關器械(代碼:MUH)
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
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。
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