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FDA 510(k)

Layer 7-T

N.º K: K242618 · 2025-03-30

SolicitantePrecision Neuroscience, Corp.
Fecha de decisión2025-03-30
Código de productoGYC
Comité asesorNE
DecisiónSubstantially Equivalent

Resumen del dispositivo

Layer 7-T is the device name listed in this FDA 510(k) record. The listed applicant is Precision Neuroscience, Corp.. It received FDA 510(k) clearance on 2025-03-30 under 510(k) number K242618. The device is classified under product code GYC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Layer 7-T?

Layer 7-T is a medical device that received FDA 510(k) clearance on 2025-03-30. The listed applicant is Precision Neuroscience, Corp.. The 510(k) number is K242618.

When did Layer 7-T receive FDA 510(k) clearance?

Layer 7-T received FDA 510(k) clearance on 2025-03-30, under 510(k) number K242618.

Who is the listed applicant for Layer 7-T?

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

What is the FDA product code for Layer 7-T?

The FDA product code for Layer 7-T is GYC.

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Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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