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FDA 510(k)

ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test

N.º K: K243064 · 2024-11-20

SolicitanteEterbio, Inc.
Fecha de decisión2024-11-20
Código de productoNGL
Comité asesorTX
DecisiónSubstantially Equivalent

Resumen del dispositivo

ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test is the device name listed in this FDA 510(k) record. The listed applicant is Eterbio, Inc.. It received FDA 510(k) clearance on 2024-11-20 under 510(k) number K243064. The device is classified under product code NGL. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test?

ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test is a medical device that received FDA 510(k) clearance on 2024-11-20. The listed applicant is Eterbio, Inc.. The 510(k) number is K243064.

When did ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test receive FDA 510(k) clearance?

ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test received FDA 510(k) clearance on 2024-11-20, under 510(k) number K243064.

Who is the listed applicant for ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test?

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

What is the FDA product code for ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test?

The FDA product code for ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test is NGL.

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Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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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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