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CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261

Page Type
Cleared 510(K)
510(k) Number
K070311
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2007
Days to Decision
82 days
Submission Type
Summary

CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261

Page Type
Cleared 510(K)
510(k) Number
K070311
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2007
Days to Decision
82 days
Submission Type
Summary