Last synced on 14 November 2025 at 11:06 pm

Renuvion/J-Plasma Precise Handpiece, Renuvion/J-Plasma Precise Open handpieces, Renuvion/J-Plasma Precise Open handpieces

Page Type
Cleared 510(K)
510(k) Number
K183610
510(k) Type
Traditional
Applicant
Bovie Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2019
Days to Decision
76 days
Submission Type
Summary

Renuvion/J-Plasma Precise Handpiece, Renuvion/J-Plasma Precise Open handpieces, Renuvion/J-Plasma Precise Open handpieces

Page Type
Cleared 510(K)
510(k) Number
K183610
510(k) Type
Traditional
Applicant
Bovie Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2019
Days to Decision
76 days
Submission Type
Summary