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FDA 510(k)

Ives MR Conditional Cup Electrode

N.º K: K171102 · 2017-12-21

SolicitanteIves Egg Solutions
Fecha de decisión2017-12-21
Código de productoGXY
Comité asesorNE
DecisiónSubstantially Equivalent

Resumen del dispositivo

Ives MR Conditional Cup Electrode is the device name listed in this FDA 510(k) record. The listed applicant is Ives Egg Solutions. It received FDA 510(k) clearance on 2017-12-21 under 510(k) number K171102. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Ives MR Conditional Cup Electrode?

Ives MR Conditional Cup Electrode is a medical device that received FDA 510(k) clearance on 2017-12-21. The listed applicant is Ives Egg Solutions. The 510(k) number is K171102.

When did Ives MR Conditional Cup Electrode receive FDA 510(k) clearance?

Ives MR Conditional Cup Electrode received FDA 510(k) clearance on 2017-12-21, under 510(k) number K171102.

Who is the listed applicant for Ives MR Conditional Cup Electrode?

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

What is the FDA product code for Ives MR Conditional Cup Electrode?

The FDA product code for Ives MR Conditional Cup Electrode is GXY.

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Dispositivos relacionados (Código: GXY)

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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