FDA 510(k)

neo315

N.º K: K231133 · 2024-07-22

Fecha de decisión2024-07-22

Código de productoLNH

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

neo315 is the device name listed in this FDA 510(k) record. The listed applicant is Neoscan Solution GmbH. It received FDA 510(k) clearance on 2024-07-22 under 510(k) number K231133. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the neo315?

neo315 is a medical device that received FDA 510(k) clearance on 2024-07-22. The listed applicant is Neoscan Solution GmbH. The 510(k) number is K231133.

When did neo315 receive FDA 510(k) clearance?

neo315 received FDA 510(k) clearance on 2024-07-22, under 510(k) number K231133.

Who is the listed applicant for neo315?

The FDA 510(k) record lists Neoscan Solution GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for neo315?

The FDA product code for neo315 is LNH.

Dispositivos relacionados (Código: LNH)

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.

K261283Sistema de RM de Lucent APERTOFujifilm Corporation K261758Embrace Vision Neonatal MRI SystemAspect Imaging, Ltd.K260758MAGNETOM Free.Max; MAGNETOM Free.StarSiemens Shenzhen Magnetic Resonance , Ltd.K262622Swoop® Portable MR Imaging® SystemHyperfine, Inc.K254250MagicScan-1.5, GreenMR Serenity 1.5TXingaoyi Medical Equipment Co.,Ltd K253808AIR Recon DLGE Medical Systems

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.