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FDA 510(k)

RS85 Diagnostic Ultrasound System

K-Number: K192903 · 2020-01-06

ApplicantSamsung Medison Co., Ltd.
Decision Date2020-01-06
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RS85 Diagnostic Ultrasound System is a medical device manufactured by Samsung Medison Co., Ltd.. It received FDA 510(k) clearance on 2020-01-06 under approval number K192903. 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 RS85 Diagnostic Ultrasound System?

RS85 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2020-01-06. It is manufactured by Samsung Medison Co., Ltd.. The 510(k) number is K192903.

When was RS85 Diagnostic Ultrasound System approved by the FDA?

RS85 Diagnostic Ultrasound System received FDA 510(k) clearance on 2020-01-06, under approval number K192903.

What company makes RS85 Diagnostic Ultrasound System?

RS85 Diagnostic Ultrasound System is manufactured by Samsung Medison Co., Ltd..

What is the FDA product code for RS85 Diagnostic Ultrasound System?

The FDA product code for RS85 Diagnostic Ultrasound System is IYN.

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Other Devices by Samsung Medison Co., Ltd.

K153539RS80A Diagnostic Ultrasound System K162094RS80A Diagnostic Ultrasound System K1619555D Viewer K153529WS80A Diagnostic Ultrasound System K171048RS80A Diagnostic Ultrasound System K171070WS80A Diagnostic Ultrasound System

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Related Devices (Code: IYN)

K162845DC-40/DC-35/DC-45/DC-40S/DC-40 Pro Diagnostic Ultrasound SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. K162902ARIETTA Prologue Diagnostic Ultrasound system and TransducersHitachi , Ltd. K163138Clarius Ultrasound SystemClarius Mobile Health Corp. K163077LOGIQ E9, LOGIQ E9 XDClear 2.0GE Medical Systems Ultrasound and Primary Care Diagnostics K162583ALOKA LISENDO 880Hitachi , Ltd. K163020Xperius Ultrasound SystemPhilips Health Care

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.

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