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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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