CMS600P2 B-Ultrasound Diagnostic System
K-Number: K170856 · 2017-11-17
Device Summary
Frequently Asked Questions
What is the CMS600P2 B-Ultrasound Diagnostic System?
CMS600P2 B-Ultrasound Diagnostic System is a medical device that received FDA 510(k) clearance on 2017-11-17. It is manufactured by Contec Medical Systems Co.,Ltd. The 510(k) number is K170856.
When was CMS600P2 B-Ultrasound Diagnostic System approved by the FDA?
CMS600P2 B-Ultrasound Diagnostic System received FDA 510(k) clearance on 2017-11-17, under approval number K170856.
What company makes CMS600P2 B-Ultrasound Diagnostic System?
CMS600P2 B-Ultrasound Diagnostic System is manufactured by Contec Medical Systems Co.,Ltd.
What is the FDA product code for CMS600P2 B-Ultrasound Diagnostic System?
The FDA product code for CMS600P2 B-Ultrasound Diagnostic System is IYO.
Related Clinical Trials
Related PubMed Literature
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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.