FDA 510(k)

LOGIQ e

N.º K: K260398 · 2026-05-26

SolicitanteGE Medical Systems Ultrasound and Primary Care Diagnostics

Fecha de decisión2026-05-26

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

LOGIQ e 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 2026-05-26 under 510(k) number K260398. 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 LOGIQ e?

LOGIQ e is a medical device that received FDA 510(k) clearance on 2026-05-26. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K260398.

When did LOGIQ e receive FDA 510(k) clearance?

LOGIQ e received FDA 510(k) clearance on 2026-05-26, under 510(k) number K260398.

Who is the listed applicant for LOGIQ e?

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 LOGIQ e?

The FDA product code for LOGIQ e is IYN.

Ensayos clínicos relacionados

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

K261623EchoPAC Software Only / EchoPAC Plug-in (v211)K261313Vivid Explorer/Vivid Advanced/Vivid Focus K261835LOGIQ Focus K260673LOGIQ 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 Power K253370LOGIQ Totus K253366LOGIQ Fortis

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Dispositivos relacionados (Código: IYN)

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.