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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 19 Results
ProductCode: GEI Applicant: BOVIE MEDICAL CORPORATION Decision Date To: 05/03/2024
 
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Export all 19 Records to ExcelExport to Excel | Download Files | More About 510(k)
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renuvion apr handpiece Apyx Medical Corporation(formerly Bovie Medical Corporation) K220970 07/15/2022
renuvion dermal handpiece, renuvion dermal system Apyx Medical Corporation (formerly Bovie Medical Corporation K211652 05/25/2022
j-plasma precise flex handpiece Apyx Medical Corporation (formerly Bovie Medical Corporation K202880 01/04/2021
apyx helium plasma generator (apyx-200h/p, apyx-js3/rs3) Bovie Medical Corporation dba Apyx Medical Corporation K192867 10/31/2019
apyx plasma/rf handpiece Bovie Medical Corporation dba Apyx Medical Corporation K191542 10/11/2019
renuvion/j-plasma precise handpiece Apyx Medical Corporation(formerly Bovie Medical Corporation) K191484 07/30/2019
renuvion/j-plasma precise handpiece, renuvion/j-plasma precise open handpieces, renuvion/j-plasma precise open handpieces Bovie Medical Corporation K183610 03/12/2019
bovie j-plasma precise flex handpiece Bovie Medical Corporation K170777 05/01/2017
bovie j-plasma precise open handpiece & bovie ultimate gen 2 high frequency electrosurgical generator Bovie Medical Corporation K170188 03/08/2017
bovie 3.3mm disposable bipolar ablator 90°, aspirating and non-aspirating, bovie 2.4mm disposable bipolar ablator 55°, non-aspirating, bovie 1.8mm disposable bipolar ablator 60°, non-aspirating BOVIE MEDICAL CORPORATION K161558 07/29/2016
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