Last synced on 25 January 2026 at 3:41 am

CARDIOBLATE SURGICAL ABLATION PEN, MODEL 60811C; CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 60880

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013392
510(k) Type
Abbreviated
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2002
Days to Decision
102 days
Submission Type
Summary

CARDIOBLATE SURGICAL ABLATION PEN, MODEL 60811C; CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 60880

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013392
510(k) Type
Abbreviated
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2002
Days to Decision
102 days
Submission Type
Summary