FDA 510(k)

RIGHTEST Blood Glucose Monitoring System Max Tel

N.º K: K231192 · 2024-01-19

Fecha de decisión2024-01-19

Código de productoNBW

Comité asesorCH

DecisiónSubstantially Equivalent

Resumen del dispositivo

RIGHTEST Blood Glucose Monitoring System Max Tel is the device name listed in this FDA 510(k) record. The listed applicant is Bionime Corporation. It received FDA 510(k) clearance on 2024-01-19 under 510(k) number K231192. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the RIGHTEST Blood Glucose Monitoring System Max Tel?

RIGHTEST Blood Glucose Monitoring System Max Tel is a medical device that received FDA 510(k) clearance on 2024-01-19. The listed applicant is Bionime Corporation. The 510(k) number is K231192.

When did RIGHTEST Blood Glucose Monitoring System Max Tel receive FDA 510(k) clearance?

RIGHTEST Blood Glucose Monitoring System Max Tel received FDA 510(k) clearance on 2024-01-19, under 510(k) number K231192.

Who is the listed applicant for RIGHTEST Blood Glucose Monitoring System Max Tel?

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

What is the FDA product code for RIGHTEST Blood Glucose Monitoring System Max Tel?

The FDA product code for RIGHTEST Blood Glucose Monitoring System Max Tel is NBW. This falls under the OB/GYN category.

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Otros registros que enlistan a Bionime Corporation como solicitante

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Fuente oficial

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