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FDA 510(k)

VIDAvision

K-Number: K200990 · 2020-08-07

ApplicantVida Diagnostics, Inc.
Decision Date2020-08-07
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDAvision is a medical device manufactured by Vida Diagnostics, Inc.. It received FDA 510(k) clearance on 2020-08-07 under approval number K200990. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDAvision?

VIDAvision is a medical device that received FDA 510(k) clearance on 2020-08-07. It is manufactured by Vida Diagnostics, Inc.. The 510(k) number is K200990.

When was VIDAvision approved by the FDA?

VIDAvision received FDA 510(k) clearance on 2020-08-07, under approval number K200990.

What company makes VIDAvision?

VIDAvision is manufactured by Vida Diagnostics, Inc..

What is the FDA product code for VIDAvision?

The FDA product code for VIDAvision is JAK.

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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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