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LELTEK Ultrasound Imaging System (Model: LU700 Series)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210432
510(k) Type
Traditional
Applicant
Leltek, Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
11/3/2021
Days to Decision
264 days
Submission Type
Summary

LELTEK Ultrasound Imaging System (Model: LU700 Series)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210432
510(k) Type
Traditional
Applicant
Leltek, Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
11/3/2021
Days to Decision
264 days
Submission Type
Summary