Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

Leltek, Inc.

FDA 510(k) & PMA Approved Dispositivos — 5 products

Total de dispositivos5
Categorías0
Última decisión de la FDA
TipoNúmeroNombre del dispositivoCódigoFechaAcciones
510(k) K243226 Ultrasound Imaging System (LU700 Series); Ultrasound Imaging System (128 Series); Ultrasound Imaging System (LX Series)IYN2025-05-08 Ver
510(k) K241161 Ultrasound Imaging System (LK128L); Ultrasound Imaging System (LK128LH); Ultrasound Imaging System (LK128C); Ultrasound Imaging System (LK128M); Ultrasound Imaging System (LK128PA); Ultrasound Imaging System (LK128E); Ultrasound Imaging System (LU700C); Ultrasound Imaging System (LU700L); Ultrasound Imaging System (LU710L); Ultrasound Imaging System (LU710LH); Ultrasound Imaging System (LU710C); Ultrasound Imaging System (LU710M); Ultrasound Imaging System (LU710PA); Ultrasound ImagingIYN2024-09-11 Ver
510(k) K222365 Leltek Ultrasound Imaging System (Model: LU700 Series)IYN2022-10-25 Ver
510(k) K210432 LELTEK Ultrasound Imaging System (Model: LU700 Series)IYN2021-11-03 Ver
510(k) K191235 Leltek Ultrasound Imaging SystemIYN2020-02-12 Ver
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