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FDA 510(k)

S60 Series Digital Color Doppler Ultrasound System

K-Number: K172082 · 2017-09-21

Decision Date2017-09-21
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

S60 Series Digital Color Doppler Ultrasound System is a medical device manufactured by Sonoscape Medical Corp.. It received FDA 510(k) clearance on 2017-09-21 under approval number K172082. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the S60 Series Digital Color Doppler Ultrasound System?

S60 Series Digital Color Doppler Ultrasound System is a medical device that received FDA 510(k) clearance on 2017-09-21. It is manufactured by Sonoscape Medical Corp.. The 510(k) number is K172082.

When was S60 Series Digital Color Doppler Ultrasound System approved by the FDA?

S60 Series Digital Color Doppler Ultrasound System received FDA 510(k) clearance on 2017-09-21, under approval number K172082.

What company makes S60 Series Digital Color Doppler Ultrasound System?

S60 Series Digital Color Doppler Ultrasound System is manufactured by Sonoscape Medical Corp..

What is the FDA product code for S60 Series Digital Color Doppler Ultrasound System?

The FDA product code for S60 Series Digital Color Doppler Ultrasound System is IYN.

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Official Source

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