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FDA 510(k)

Venue; Venue Go; Venue Fit; Venue Sprint

N.º K: K251322 · 2025-07-25

SolicitanteGE Medical Systems Ultrasound and Primary Care Diagnostics
Fecha de decisión2025-07-25
Código de productoIYN
Comité asesorRA
DecisiónSubstantially Equivalent

Resumen del dispositivo

Venue; Venue Go; Venue Fit; Venue Sprint is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. It received FDA 510(k) clearance on 2025-07-25 under 510(k) number K251322. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Venue; Venue Go; Venue Fit; Venue Sprint?

Venue; Venue Go; Venue Fit; Venue Sprint is a medical device that received FDA 510(k) clearance on 2025-07-25. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K251322.

When did Venue; Venue Go; Venue Fit; Venue Sprint receive FDA 510(k) clearance?

Venue; Venue Go; Venue Fit; Venue Sprint received FDA 510(k) clearance on 2025-07-25, under 510(k) number K251322.

Who is the listed applicant for Venue; Venue Go; Venue Fit; Venue Sprint?

The FDA 510(k) record lists GE Medical Systems Ultrasound and Primary Care Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Venue; Venue Go; Venue Fit; Venue Sprint?

The FDA product code for Venue; Venue Go; Venue Fit; Venue Sprint is IYN.

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Otros registros que enlistan a GE Medical Systems Ultrasound and Primary Care Diagnostics como solicitante

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K261623EchoPAC Software Only / EchoPAC Plug-in (v211)K261313Vivid Explorer/Vivid Advanced/Vivid FocusK261835LOGIQ FocusK260398LOGIQ eK260673LOGIQ Vita; LOGIQ Vita Pro; LOGIQ Vita Express; LOGIQ Vita Plus; LOGIQ Vita Power; LOGIQ S20; LOGIQ S20 Pro; LOGIQ S20 Express; LOGIQ S20 Plus; LOGIQ S20 PowerK253370LOGIQ Totus

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Dispositivos relacionados (Código: IYN)

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.

K263182EVO X30 Diagnostic Ultrasound System; EVO X20 Diagnostic Ultrasound System; EVO X10 Diagnostic Ultrasound System; EVO XP30 Diagnostic Ultrasound System; EVO XP20 Diagnostic Ultrasound System; EVO XP10 Diagnostic Ultrasound System; EVO XC30 Diagnostic Ultrasound System; EVO XC20 Diagnostic Ultrasound System; EVO XC10 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.K262548EPIQ Inspira Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound SystemPhilips Ultrasound, LLCK261313Vivid Explorer/Vivid Advanced/Vivid FocusGE Medical Systems Ultrasound and Primary Care DiagnosticsK254027Digital Color Doppler Ultrasound System (Marvo 95/Marvo 95 Elite/Marvo 90/Marvo 90 CV/Marvo 90 Pro/Marvo 90 Exp/Marvo 90 Elite/Marvo Expert/Marvo 85/Marvo 85 Pro/Marvo 85 Exp/Marvo 85 Elite/Marvo Senior/Marvo 75 Elite/Marvo 75i/Fenix 95/Fenix 95 Elite/Fenix 90/Fenix 90 Elite/Fenix Expert/Fenix 85/Fenix 85 Elite/Fenix Senior/Fenix 75 Elite/Fenix 75i/Endo 80/Endo 90)Sonoscape Medical Corp.K261668Venue GoGE Medical Systems Ultrasound and Primary care Diagnostics, LLCK262311Sistema de Ultrasonido Diagnóstico de la Serie AlturionPhilips Ultrasound, LLC

Fuente oficial

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