FDA 510(k)

BD Phoenix™ Automated Microbiology System

N.º K: K250344 · 2025-03-06

SolicitanteBecton, Dickinson and Company

Fecha de decisión2025-03-06

Código de productoLON

Comité asesorMI

DecisiónSubstantially Equivalent

Resumen del dispositivo

BD Phoenix™ Automated Microbiology System is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2025-03-06 under 510(k) number K250344. The device is classified under product code LON. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the BD Phoenix™ Automated Microbiology System?

BD Phoenix™ Automated Microbiology System is a medical device that received FDA 510(k) clearance on 2025-03-06. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K250344.

When did BD Phoenix™ Automated Microbiology System receive FDA 510(k) clearance?

BD Phoenix™ Automated Microbiology System received FDA 510(k) clearance on 2025-03-06, under 510(k) number K250344.

Who is the listed applicant for BD Phoenix™ Automated Microbiology System?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Phoenix™ Automated Microbiology System?

The FDA product code for BD Phoenix™ Automated Microbiology System is LON.

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Fuente oficial

Ver en la base de datos de la FDA →

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