FDA 510(k) Applications Submitted by Apyx Medical Corporation(formerly Bovie Medical Corporation)

FDA 510(k) Number Submission Date Device Name Applicant
K220970 04/04/2022 Renuvion APR Handpiece Apyx Medical Corporation(formerly Bovie Medical Corporation)
K191484 06/04/2019 Renuvion/J-Plasma Precise Handpiece Apyx Medical Corporation(formerly Bovie Medical Corporation)


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