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EPi-Ease Epicardial Access Device (EAS)

Page Type
Cleared 510(K)
510(k) Number
K233959
510(k) Type
Traditional
Applicant
Atricure, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2024
Days to Decision
60 days
Submission Type
Summary

EPi-Ease Epicardial Access Device (EAS)

Page Type
Cleared 510(K)
510(k) Number
K233959
510(k) Type
Traditional
Applicant
Atricure, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2024
Days to Decision
60 days
Submission Type
Summary