Last synced on 25 January 2026 at 3:41 am

BOVIE MODEL X15

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972161
510(k) Type
Traditional
Applicant
Maxxim Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1997
Days to Decision
9 days
Submission Type
Statement

BOVIE MODEL X15

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972161
510(k) Type
Traditional
Applicant
Maxxim Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/1997
Days to Decision
9 days
Submission Type
Statement