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Valleylab FT10 Electrosurgical Platform, Cardioblate BP2 Surgical Ablation Device, Cardioblate LP Surgical Ablation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182610
510(k) Type
Traditional
Applicant
Medtronic
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2018
Days to Decision
89 days
Submission Type
Summary

Valleylab FT10 Electrosurgical Platform, Cardioblate BP2 Surgical Ablation Device, Cardioblate LP Surgical Ablation Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182610
510(k) Type
Traditional
Applicant
Medtronic
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2018
Days to Decision
89 days
Submission Type
Summary