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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 the device name listed in this FDA 510(k) record. The listed applicant is Qstag, Inc.. It received FDA 510(k) clearance on 2026-02-20 under 510(k) 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. The listed applicant is Qstag, Inc.. The 510(k) number is K252619.

When did QSCHECK UISACR receive FDA 510(k) clearance?

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

Who is the listed applicant for QSCHECK UISACR?

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

What is the FDA product code for QSCHECK UISACR?

The FDA product code for QSCHECK UISACR is JFY.

Related Devices (Code: JFY)

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.

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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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