FDA 510(k) Applications Submitted by Enraf-Nonius, B.V.

FDA 510(k) Number Submission Date Device Name Applicant
K230472 02/22/2023 Sonopuls 190 Enraf-Nonius, B.V.
K243112 09/30/2024 Curapuls 670 Enraf-Nonius, B.V.


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