FDA 510(k)

CFP-3131, CFP-2222

N.º K: K201172 · 2020-05-29

Fecha de decisión2020-05-29

Código de productoOWB

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

CFP-3131, CFP-2222 is the device name listed in this FDA 510(k) record. The listed applicant is Mx Imaging, Inc.. It received FDA 510(k) clearance on 2020-05-29 under 510(k) number K201172. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CFP-3131, CFP-2222?

CFP-3131, CFP-2222 is a medical device that received FDA 510(k) clearance on 2020-05-29. The listed applicant is Mx Imaging, Inc.. The 510(k) number is K201172.

When did CFP-3131, CFP-2222 receive FDA 510(k) clearance?

CFP-3131, CFP-2222 received FDA 510(k) clearance on 2020-05-29, under 510(k) number K201172.

Who is the listed applicant for CFP-3131, CFP-2222?

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

What is the FDA product code for CFP-3131, CFP-2222?

The FDA product code for CFP-3131, CFP-2222 is OWB.

Dispositivos relacionados (Código: OWB)

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.

K253726uAngio AVIVA CXShanghai United Imaging Healthcare Co., Ltd.K261413EXTRON 3;EXTRON 6DRTECH Corporation K254205Zenition 30Philips Medical Systems Nederland B.V.K260607Shield System (Siemens 30x40)Radiaction , Ltd.K253670SmartCT (R3.0 (L10))Philips Medical Systems B.V.K252735C-beamPulmera, Inc.

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.