FDA 510(k)

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))

N.º K: K252160 · 2025-10-31

Fecha de decisión2025-10-31

Código de productoOMB

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) is the device name listed in this FDA 510(k) record. The listed applicant is Persyst Development, LLC. It received FDA 510(k) clearance on 2025-10-31 under 510(k) number K252160. The device is classified under product code OMB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))?

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) is a medical device that received FDA 510(k) clearance on 2025-10-31. The listed applicant is Persyst Development, LLC. The 510(k) number is K252160.

When did Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) receive FDA 510(k) clearance?

Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) received FDA 510(k) clearance on 2025-10-31, under 510(k) number K252160.

Who is the listed applicant for Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))?

The FDA 510(k) record lists Persyst Development, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))?

The FDA product code for Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) is OMB.

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: OMB)

K260998Ceribell Neurology Review SoftwareCeribell, Inc.K252070Ceribell Infant Seizure Detection SoftwareCeribell, Inc.K243743autoSCORE (V 2.0.0)Holberg Eeg AS K241589Ceribell Seizure Detection SoftwareCeribell, Inc.K242446Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15))Persyst Development Corporation K241390NeuroMatchLVIS Corporation

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.