FDA 510(k) Applications Submitted by Pristine Surgical

FDA 510(k) Number Submission Date Device Name Applicant
K223244 10/20/2022 Pristine Arthroscopic Visualization System Pristine Surgical
K183165 11/15/2018 Pristine Scope Pristine Surgical
K193161 11/15/2019 Pristine Scope Pristine Surgical


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