FDA 510(k)

LOGIQ V1/ LOGIQ V2

K 號：K153037 · 2016-01-04

申請人GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC

決定日期2016-01-04

產品代碼IYN

諮詢委員會RA

決定Substantially Equivalent

器材摘要

LOGIQ V1/ LOGIQ V2 is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC. It received FDA 510(k) clearance on 2016-01-04 under 510(k) number K153037. 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 LOGIQ V1/ LOGIQ V2?

LOGIQ V1/ LOGIQ V2 is a medical device that received FDA 510(k) clearance on 2016-01-04. The listed applicant is GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC. The 510(k) number is K153037.

When did LOGIQ V1/ LOGIQ V2 receive FDA 510(k) clearance?

LOGIQ V1/ LOGIQ V2 received FDA 510(k) clearance on 2016-01-04, under 510(k) number K153037.

Who is the listed applicant for LOGIQ V1/ LOGIQ V2?

The FDA 510(k) record lists GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOGIQ V1/ LOGIQ V2?

The FDA product code for LOGIQ V1/ LOGIQ V2 is IYN.

其他以 GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC 為申請人之記錄

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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。

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