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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