FDA 510(k)

Vivid iq

K 號：K161706 · 2016-08-05

申請人Ge Medical Systems Ultrasound and Primary Care Diagnostics L

決定日期2016-08-05

產品代碼IYN

諮詢委員會RA

決定相當於

器材摘要

Vivid iq is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Ultrasound and Primary Care Diagnostics L. It received FDA 510(k) clearance on 2016-08-05 under 510(k) number K161706. 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 Vivid iq?

Vivid iq is a medical device that received FDA 510(k) clearance on 2016-08-05. The listed applicant is Ge Medical Systems Ultrasound and Primary Care Diagnostics L. The 510(k) number is K161706.

When did Vivid iq receive FDA 510(k) clearance?

Vivid iq received FDA 510(k) clearance on 2016-08-05, under 510(k) number K161706.

Who is the listed applicant for Vivid iq?

The FDA 510(k) record lists Ge Medical Systems Ultrasound and Primary Care Diagnostics L as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vivid iq?

The FDA product code for Vivid iq is IYN.

相關器械（代碼：IYN）

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：IYN）

官方來源