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FDA 510(k)

CMS600P2 B-Ultrasound Diagnostic System

K-Number: K170856 · 2017-11-17

Decision Date2017-11-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CMS600P2 B-Ultrasound Diagnostic System is a medical device manufactured by Contec Medical Systems Co.,Ltd. It received FDA 510(k) clearance on 2017-11-17 under approval number K170856. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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