FDA 510(k)

QSCHECK UISACR

N.º K: K252619 · 2026-02-20

Fecha de decisión2026-02-20

Código de productoJFY

Comité asesorCH

DecisiónSubstantially Equivalent

Resumen del dispositivo

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.

Preguntas frecuentes

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.

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Fuente oficial

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