FDA 510(k)

Multimodality Simulation Workspace (MM Sim) (v1.0.0)

N.º K: K260207 · 2026-05-27

SolicitantePhilips Medical Systems Nederland B.V.

Fecha de decisión2026-05-27

Código de productoMUJ

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Multimodality Simulation Workspace (MM Sim) (v1.0.0) is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2026-05-27 under 510(k) number K260207. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Multimodality Simulation Workspace (MM Sim) (v1.0.0)?

Multimodality Simulation Workspace (MM Sim) (v1.0.0) is a medical device that received FDA 510(k) clearance on 2026-05-27. The listed applicant is Philips Medical Systems Nederland B.V.. The 510(k) number is K260207.

When did Multimodality Simulation Workspace (MM Sim) (v1.0.0) receive FDA 510(k) clearance?

Multimodality Simulation Workspace (MM Sim) (v1.0.0) received FDA 510(k) clearance on 2026-05-27, under 510(k) number K260207.

Who is the listed applicant for Multimodality Simulation Workspace (MM Sim) (v1.0.0)?

The FDA 510(k) record lists Philips Medical Systems Nederland B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multimodality Simulation Workspace (MM Sim) (v1.0.0)?

The FDA product code for Multimodality Simulation Workspace (MM Sim) (v1.0.0) is MUJ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Otros registros que enlistan a Philips Medical Systems Nederland B.V. como solicitante

K254205Zenition 30 K262330dS Breast 7ch 1.5TdS Breast 7ch 3.0TdS Breast 16ch 1.5TdS Breast 16ch 3.0TdS Breast Coil 7ch 1.5TdS Sentinelle Breast 16ch 1.5TdS Sentinelle Breast 16ch 3.0T K262294dS FootAnkle 16Ch 1.5T;dS FootAnkle 16Ch 3.0T;dS HiRes Hand/Wrist 16Ch 1.5T;dS HiRes Hand/Wrist 16CH 3.0T;dS Small Extremity 16Ch 1.5T;dS Small Extremity 16Ch 3.0T K253614EchoNavigator R5.0 K260169AV Cardiac CT K253648Ingenia, Ingenia CX, Ingenia Elition S/X, Ingenia Ambition S/X, BlueSeal SE/XE/QE, MR 5300 and MR 7700 MR Systems including Upgrades

Ver todos los 80 dispositivos →

Dispositivos relacionados (Código: MUJ)

K260750Virtual Cone (1.0)Varian Medical Systems, Inc.K253050RadOncAIInformai K252784eXaSkin PlusAnatomical Geometry S.L.K253078ART.1-USSeetreat Pty, Ltd.K252304syngo.via RT Image Suite VC10Varian Medical Systems, Inc.K252002Monaco RTP System (6.3)Elekta Solutions AB

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.