FDA 510(k)

Virasight

K-Number: K251952 · 2026-07-17

Decision Date2026-07-17

Product CodePSY

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

Virasight is the device name listed in this FDA 510(k) record. The listed applicant is Virasoft Corporation. It received FDA 510(k) clearance on 2026-07-17 under 510(k) number K251952. The device is classified under product code PSY. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Virasight?

Virasight is a medical device that received FDA 510(k) clearance on 2026-07-17. The listed applicant is Virasoft Corporation. The 510(k) number is K251952.

When did Virasight receive FDA 510(k) clearance?

Virasight received FDA 510(k) clearance on 2026-07-17, under 510(k) number K251952.

Who is the listed applicant for Virasight?

The FDA 510(k) record lists Virasoft Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Virasight?

The FDA product code for Virasight is PSY.

Related Devices (Code: PSY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253606NanoZoomer S20MD Slide scanner system; NanoZoomer S360MD Slide scanner systemHamamatsu Photonics K.K.K243871Philips IntelliSite Pathology Solution 5.1Philips Medical Systems Nederland B.V.K241717E1000 Dx Digital Pathology SolutionShandon Diagnostics Limited K242783Roche Digital Pathology DxVentana Medical Systems, Inc.K242848Philips IntelliSite Pathology Solution 5.1Philips Medical Systems Nederland B.V.K241871Philips IntelliSite Pathology SolutionPhilips Medical Systems Nederland B.V.

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.