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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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