FDA 510(k)

ACUSON S1000/S2000/S3000診断超音波システム

K番号: K163635 · 2017-01-12

申請者Siemens Medical Solutions USA, Inc. Ultrasound Group

決定日2017-01-12

製品コードIYN

諮問委員会RA （注：由于原文中未提供具体的医疗设备监管文本内容，因此无法进行翻译。请提供具体的文本内容以便进行翻译。）

決定大幅同等

医療機器の概要

ACUSON S1000/S2000/S3000 Diagnostic Ultrasound Systems is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc. Ultrasound Group. It received FDA 510(k) clearance on 2017-01-12 under 510(k) number K163635. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the ACUSON S1000/S2000/S3000 Diagnostic Ultrasound Systems?

ACUSON S1000/S2000/S3000 Diagnostic Ultrasound Systems is a medical device that received FDA 510(k) clearance on 2017-01-12. The listed applicant is Siemens Medical Solutions USA, Inc. Ultrasound Group. The 510(k) number is K163635.

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

ACUSON S1000/S2000/S3000 Diagnostic Ultrasound Systems received FDA 510(k) clearance on 2017-01-12, under 510(k) number K163635.

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

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. Ultrasound Group 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 Systems?

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

申請者としてSiemens Medical Solutions USA, Inc. Ultrasound Groupを記載するその他の記録

K173981ACUSON NX2診断超音波システム、ACUSON NX2 エリート診断超音波システム

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