Last synced on 17 January 2025 at 11:05 pm

Bovie J-Plasma Precise FLEX Handpiece

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170777
510(k) Type
Traditional
Applicant
Bovie Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2017
Days to Decision
47 days
Submission Type
Summary