ACUSON S1000/S2000/S3000 Diagnostic Ultrasound Systems
K-Number: K163635 · 2017-01-12
Device Summary
Frequently Asked Questions
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.
Other records listing Siemens Medical Solutions USA, Inc. Ultrasound Group as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IYN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.