Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VIVIX-S VW

K-Number: K200418 · 2020-03-18

ApplicantVieworks Co., Ltd.
Decision Date2020-03-18
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIVIX-S VW is a medical device manufactured by Vieworks Co., Ltd.. It received FDA 510(k) clearance on 2020-03-18 under approval number K200418. 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 VW?

VIVIX-S VW is a medical device that received FDA 510(k) clearance on 2020-03-18. It is manufactured by Vieworks Co., Ltd.. The 510(k) number is K200418.

When was VIVIX-S VW approved by the FDA?

VIVIX-S VW received FDA 510(k) clearance on 2020-03-18, under approval number K200418.

What company makes VIVIX-S VW?

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

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

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

Other Devices by Vieworks Co., Ltd.

K161113QXLink K152894VIVIX-S 1717N K152855VIVIX-S 1012N K163703VIVIX-S 1417N K181003VIVIX-S 1717V K190611VIVIX-S 1751S

View all 12 devices →

Related Devices (Code: MQB)

K162555EVS 4343, EVS 4343GDRTECH Corporation K162344INNOLUX RICInnolux Corporation K161730Wireless Digital Flat Panel DetectorIray Technology (Shanghai) , Ltd. K162552EVS 3643, EVS 3643GDRTECH Corporation K163019CareView 750Cw/750C X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. K160143ClearVision ExamVue Flat Panel DetectorJpi Healthcare, Inc.

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.

↑