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CRF Radiofrequency Ablation System

Page Type
Cleared 510(K)
510(k) Number
K192715
510(k) Type
Traditional
Applicant
Cambridge Interventional LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2020
Days to Decision
102 days
Submission Type
Summary

CRF Radiofrequency Ablation System

Page Type
Cleared 510(K)
510(k) Number
K192715
510(k) Type
Traditional
Applicant
Cambridge Interventional LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2020
Days to Decision
102 days
Submission Type
Summary