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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 the device name listed in this FDA 510(k) record. The listed applicant is Vida Diagnostics, Inc.. It received FDA 510(k) clearance on 2020-08-07 under 510(k) 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. The listed applicant is Vida Diagnostics, Inc.. The 510(k) number is K200990.

When did VIDAvision receive FDA 510(k) clearance?

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

Who is the listed applicant for VIDAvision?

The FDA 510(k) record lists Vida Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIDAvision?

The FDA product code for VIDAvision is JAK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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