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FDA 510(k)

VIVIX-S 1751S

K-Number: K190611 · 2019-04-08

ApplicantVieworks Co., Ltd.
Decision Date2019-04-08
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIVIX-S 1751S is a medical device manufactured by Vieworks Co., Ltd.. It received FDA 510(k) clearance on 2019-04-08 under approval number K190611. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIVIX-S 1751S?

VIVIX-S 1751S is a medical device that received FDA 510(k) clearance on 2019-04-08. It is manufactured by Vieworks Co., Ltd.. The 510(k) number is K190611.

When was VIVIX-S 1751S approved by the FDA?

VIVIX-S 1751S received FDA 510(k) clearance on 2019-04-08, under approval number K190611.

What company makes VIVIX-S 1751S?

VIVIX-S 1751S is manufactured by Vieworks Co., Ltd..

What is the FDA product code for VIVIX-S 1751S?

The FDA product code for VIVIX-S 1751S is MQB.

Other Devices by Vieworks Co., Ltd.

K161113QXLink K152894VIVIX-S 1717N K152855VIVIX-S 1012N K163703VIVIX-S 1417N K181003VIVIX-S 1717V K200418VIVIX-S VW

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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.

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