FDA 510(k)

ACUSON S1000 / S2000 / S3000 診斷超音波系統

K 號：K162243 · 2016-09-06

決定日期2016-09-06

產品代碼IYN

諮詢委員會RA

決定相當於

器材摘要

ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medi Cal Solutions, Inc.. It received FDA 510(k) clearance on 2016-09-06 under 510(k) number K162243. 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 ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System?

ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2016-09-06. The listed applicant is Siemens Medi Cal Solutions, Inc.. The 510(k) number is K162243.

When did ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System receive FDA 510(k) clearance?

ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System received FDA 510(k) clearance on 2016-09-06, under 510(k) number K162243.

Who is the listed applicant for ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System?

The FDA 510(k) record lists Siemens Medi Cal Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System?

The FDA product code for ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System is IYN.

其他以 Siemens Medi Cal Solutions, Inc. 為申請人之記錄

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相關器械（代碼：IYN）

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