FDA 510(k) Applications Submitted by Leltek Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K241161 04/26/2024 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); U Leltek Inc.
K243226 10/08/2024 Ultrasound Imaging System (LU700 Series); Ultrasound Imaging System (128 Series); Ultrasound Imaging System (LX Series) Leltek Inc.


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