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Eblator Device

Page Type
Cleared 510(K)
510(k) Number
K231126
510(k) Type
Traditional
Applicant
E Surgical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2023
Days to Decision
104 days
Submission Type
Summary

Eblator Device

Page Type
Cleared 510(K)
510(k) Number
K231126
510(k) Type
Traditional
Applicant
E Surgical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2023
Days to Decision
104 days
Submission Type
Summary