Last synced on 10 January 2025 at 11:05 pm

Eblator Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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