FDA 510(k)

Dolphin Medical Imaging USB Ultrasound System

N.º K: K192573 · 2019-11-19

Fecha de decisión2019-11-19

Código de productoIYO

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Dolphin Medical Imaging USB Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Dolphin Medical Imaging, LLC. It received FDA 510(k) clearance on 2019-11-19 under 510(k) number K192573. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Dolphin Medical Imaging USB Ultrasound System?

Dolphin Medical Imaging USB Ultrasound System is a medical device that received FDA 510(k) clearance on 2019-11-19. The listed applicant is Dolphin Medical Imaging, LLC. The 510(k) number is K192573.

When did Dolphin Medical Imaging USB Ultrasound System receive FDA 510(k) clearance?

Dolphin Medical Imaging USB Ultrasound System received FDA 510(k) clearance on 2019-11-19, under 510(k) number K192573.

Who is the listed applicant for Dolphin Medical Imaging USB Ultrasound System?

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

What is the FDA product code for Dolphin Medical Imaging USB Ultrasound System?

The FDA product code for Dolphin Medical Imaging USB Ultrasound System is IYO.

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: IYO)

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApS K252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, Inc.

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.