ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System
K-Number: K162243 · 2016-09-06
Device Summary
Frequently Asked Questions
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. It is manufactured by Siemens Medi Cal Solutions, Inc.. The 510(k) number is K162243.
When was ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System approved by the FDA?
ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System received FDA 510(k) clearance on 2016-09-06, under approval number K162243.
What company makes ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System?
ACUSON S1000 / S2000 / S3000 Diagnostic Ultrasound System is manufactured by Siemens Medi Cal Solutions, Inc..
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.
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Official Source
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