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FDA 510(k)

PRESSUREALERT® Pressure Monitoring System

N.º K: K233096 · 2024-06-21

SolicitantePosition Health, LLC
Fecha de decisión2024-06-21
Código de productoSBO
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

PRESSUREALERT® Pressure Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Position Health, LLC. It received FDA 510(k) clearance on 2024-06-21 under 510(k) number K233096. The device is classified under product code SBO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the PRESSUREALERT® Pressure Monitoring System?

PRESSUREALERT® Pressure Monitoring System is a medical device that received FDA 510(k) clearance on 2024-06-21. The listed applicant is Position Health, LLC. The 510(k) number is K233096.

When did PRESSUREALERT® Pressure Monitoring System receive FDA 510(k) clearance?

PRESSUREALERT® Pressure Monitoring System received FDA 510(k) clearance on 2024-06-21, under 510(k) number K233096.

Who is the listed applicant for PRESSUREALERT® Pressure Monitoring System?

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

What is the FDA product code for PRESSUREALERT® Pressure Monitoring System?

The FDA product code for PRESSUREALERT® Pressure Monitoring System is SBO.

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Fuente oficial

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