FDA 510(k)

MuscleView 2.0

N.º K: K251682 · 2025-09-09

SolicitanteSpringbok, Inc. (Dba Springbok Analytics)

Fecha de decisión2025-09-09

Código de productoLNH

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

MuscleView 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Springbok, Inc. (Dba Springbok Analytics). It received FDA 510(k) clearance on 2025-09-09 under 510(k) number K251682. 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 MuscleView 2.0?

MuscleView 2.0 is a medical device that received FDA 510(k) clearance on 2025-09-09. The listed applicant is Springbok, Inc. (Dba Springbok Analytics). The 510(k) number is K251682.

When did MuscleView 2.0 receive FDA 510(k) clearance?

MuscleView 2.0 received FDA 510(k) clearance on 2025-09-09, under 510(k) number K251682.

Who is the listed applicant for MuscleView 2.0?

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

What is the FDA product code for MuscleView 2.0?

The FDA product code for MuscleView 2.0 is LNH.

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

Dispositivos relacionados (Código: LNH)

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.