Last synced on 14 November 2025 at 11:06 pm

Renuvion APR Handpiece

Page Type
Cleared 510(K)
510(k) Number
K220970
510(k) Type
Traditional
Applicant
Apyx Medical Corporation(formerly Bovie Medical Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
102 days
Submission Type
Summary

Renuvion APR Handpiece

Page Type
Cleared 510(K)
510(k) Number
K220970
510(k) Type
Traditional
Applicant
Apyx Medical Corporation(formerly Bovie Medical Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
102 days
Submission Type
Summary