Last synced on 10 January 2025 at 11:05 pm

CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000; CARDIOBLATE BP2 SURGICAL ABLATION DEVICE, MODEL 60831; CARDIOBLAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060400
510(k) Type
Traditional
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2006
Days to Decision
13 days
Submission Type
Summary

CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000; CARDIOBLATE BP2 SURGICAL ABLATION DEVICE, MODEL 60831; CARDIOBLAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060400
510(k) Type
Traditional
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2006
Days to Decision
13 days
Submission Type
Summary