ACUSON S3000, S2000 Diagnostic Ultrasound System
K-Number: K183575 · 2019-03-20
Device Summary
Frequently Asked Questions
What is the ACUSON S3000, S2000 Diagnostic Ultrasound System?
ACUSON S3000, S2000 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2019-03-20. The listed applicant is Siemens Healthineers. The 510(k) number is K183575.
When did ACUSON S3000, S2000 Diagnostic Ultrasound System receive FDA 510(k) clearance?
ACUSON S3000, S2000 Diagnostic Ultrasound System received FDA 510(k) clearance on 2019-03-20, under 510(k) number K183575.
Who is the listed applicant for ACUSON S3000, S2000 Diagnostic Ultrasound System?
The FDA 510(k) record lists Siemens Healthineers as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACUSON S3000, S2000 Diagnostic Ultrasound System?
The FDA product code for ACUSON S3000, S2000 Diagnostic Ultrasound System is IYN.
Other records listing Siemens Healthineers 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.