FDA 510(k)

美迪森超音波診斷成像系統，型號P1、P3及P10

K 號：K163688 · 2017-02-23

決定日期2017-02-23

產品代碼IYN

諮詢委員會RA

決定相當於

器材摘要

Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10 is the device name listed in this FDA 510(k) record. The listed applicant is Medisono, LLC. It received FDA 510(k) clearance on 2017-02-23 under 510(k) number K163688. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10?

Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10 is a medical device that received FDA 510(k) clearance on 2017-02-23. The listed applicant is Medisono, LLC. The 510(k) number is K163688.

When did Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10 receive FDA 510(k) clearance?

Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10 received FDA 510(k) clearance on 2017-02-23, under 510(k) number K163688.

Who is the listed applicant for Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10?

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

What is the FDA product code for Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10?

The FDA product code for Medisono Ultrasonic Diagnostic Imaging System, models P1, P3, and P10 is IYN.

其他以 Medisono, LLC 為申請人之記錄

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K170078美迪生彩色多普勒超音波系統，型號P11便携式、P11 EXPERT便携式、P12推車式、P12 Expert、P25推車式以及P25 Expert推車式

相關器械（代碼：IYN）

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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