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FDA 510(k)

PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software

N.º K: K240276 · 2024-05-10

Fecha de decisión2024-05-10
Código de productoNEZ
Comité asesorGU
DecisiónSubstantially Equivalent

Resumen del dispositivo

PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software is the device name listed in this FDA 510(k) record. The listed applicant is Given Imaging Ltd. (D.B.A. Medtronic). It received FDA 510(k) clearance on 2024-05-10 under 510(k) number K240276. The device is classified under product code NEZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software?

PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software is a medical device that received FDA 510(k) clearance on 2024-05-10. The listed applicant is Given Imaging Ltd. (D.B.A. Medtronic). The 510(k) number is K240276.

When did PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software receive FDA 510(k) clearance?

PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software received FDA 510(k) clearance on 2024-05-10, under 510(k) number K240276.

Who is the listed applicant for PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software?

The FDA 510(k) record lists Given Imaging Ltd. (D.B.A. Medtronic) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software?

The FDA product code for PillCam™ Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software is NEZ.

Ensayos clínicos relacionados

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.

Dispositivos relacionados (Código: NEZ)

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.

Fuente oficial

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