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Emprint SX Ablation Platform and Accessories

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171358
510(k) Type
Traditional
Applicant
Coviden, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2017
Days to Decision
115 days
Submission Type
Summary

Emprint SX Ablation Platform and Accessories

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171358
510(k) Type
Traditional
Applicant
Coviden, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2017
Days to Decision
115 days
Submission Type
Summary