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FDA 510(k)

QSCHECK UISACR

K-Number: K252619 · 2026-02-20

ApplicantQstag, Inc.
Decision Date2026-02-20
Product CodeJFY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QSCHECK UISACR is a medical device manufactured by Qstag, Inc.. It received FDA 510(k) clearance on 2026-02-20 under approval number K252619. The device is classified under product code JFY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QSCHECK UISACR?

QSCHECK UISACR is a medical device that received FDA 510(k) clearance on 2026-02-20. It is manufactured by Qstag, Inc.. The 510(k) number is K252619.

When was QSCHECK UISACR approved by the FDA?

QSCHECK UISACR received FDA 510(k) clearance on 2026-02-20, under approval number K252619.

What company makes QSCHECK UISACR?

QSCHECK UISACR is manufactured by Qstag, Inc..

What is the FDA product code for QSCHECK UISACR?

The FDA product code for QSCHECK UISACR is JFY.

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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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