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FDA 510(k) Applications Submitted by Bovie Medical Corporation dba Apyx Medical Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191542
06/11/2019
Apyx Plasma/RF Handpiece
Bovie Medical Corporation dba Apyx Medical Corporation
K192867
10/07/2019
Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3)
Bovie Medical Corporation dba Apyx Medical Corporation
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