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. It is manufactured by Siemens Healthineers. The 510(k) number is K183575.
When was ACUSON S3000, S2000 Diagnostic Ultrasound System approved by the FDA?
ACUSON S3000, S2000 Diagnostic Ultrasound System received FDA 510(k) clearance on 2019-03-20, under approval number K183575.
What company makes ACUSON S3000, S2000 Diagnostic Ultrasound System?
ACUSON S3000, S2000 Diagnostic Ultrasound System is manufactured by Siemens Healthineers.
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.
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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.