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FDA 510(k)

VINNO 8, VINNO 6, VINNO 5

K-Number: K190120 · 2020-01-23

ApplicantVinno Technology (Suzhou) Co.,Ltd
Decision Date2020-01-23
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VINNO 8, VINNO 6, VINNO 5 is a medical device manufactured by Vinno Technology (Suzhou) Co.,Ltd. It received FDA 510(k) clearance on 2020-01-23 under approval number K190120. 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 VINNO 8, VINNO 6, VINNO 5?

VINNO 8, VINNO 6, VINNO 5 is a medical device that received FDA 510(k) clearance on 2020-01-23. It is manufactured by Vinno Technology (Suzhou) Co.,Ltd. The 510(k) number is K190120.

When was VINNO 8, VINNO 6, VINNO 5 approved by the FDA?

VINNO 8, VINNO 6, VINNO 5 received FDA 510(k) clearance on 2020-01-23, under approval number K190120.

What company makes VINNO 8, VINNO 6, VINNO 5?

VINNO 8, VINNO 6, VINNO 5 is manufactured by Vinno Technology (Suzhou) Co.,Ltd.

What is the FDA product code for VINNO 8, VINNO 6, VINNO 5?

The FDA product code for VINNO 8, VINNO 6, VINNO 5 is IYN.

Other Devices by Vinno Technology (Suzhou) Co.,Ltd

K221911VINNO 6PRO, VINNO 6EXP, VINNO 5PRO, VINNO 5EXP, VINNO 3, VINNO 3PRO, VINNO 3EXP K230160VINNO G86,VINNO G86E,VINNO G65,VINNO G65P,VINNO G65E,VINNO G65D,VINNO M86, VINNO M86E,VINNO G90,VINNO G90E K223917VINNO E20, VINNO E10,VINNO E10P,VINNO E10E, VINNO X1,VINNO X1E,VINNO X1P, VINNO X2,VINNO X2E,VINNO X2P K223920VINNO G50, VINNO G55, VINNO M50, VINNO E30, VINNO X5, VINNO X6, VINNO X7, VINNO M55, VINNO E35, VINNO X65, VINNO X55, VINNO X35, VINNO G55E, VINNO G55P, VINNO M55E, VINNO M55P, VINNO E35E, VINNO E35P K240676ULTIMUS Series Ultrasound Diagnostic System

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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