FDA 510(k) Applications Submitted by Matthew Minks

FDA 510(k) Number Submission Date Device Name Applicant
K241598 06/04/2024 LithoVue Elite Single-Use Digital Flexible Ureteroscope - Standard (with pressure monitoring) (M0067940000); LithoVue Elite Single-Use Digital Flexible Ureteroscope -û Reverse (with pressure monitoring) (M0067940500); LithoVue Elite Single-Use Digital F Boston Scientific Corporation


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