Last synced on 25 January 2026 at 3:41 am

EvoEndo Single-Use Endoscopy System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213606
510(k) Type
Traditional
Applicant
EvoEndo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2022
Days to Decision
91 days
Submission Type
Summary

EvoEndo Single-Use Endoscopy System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213606
510(k) Type
Traditional
Applicant
EvoEndo, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2022
Days to Decision
91 days
Submission Type
Summary