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CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K121767
510(k) Type
Special
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2012
Days to Decision
28 days
Submission Type
Summary

CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K121767
510(k) Type
Special
Applicant
MEDTRONIC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2012
Days to Decision
28 days
Submission Type
Summary