Last synced on 23 February 2024 at 11:04 pm

DiLumen C1, EZ1 and Tool Mount

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221452
510(k) Type
Traditional
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2023
Days to Decision
268 days
Submission Type
Summary

DiLumen C1, EZ1 and Tool Mount

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221452
510(k) Type
Traditional
Applicant
Lumendi, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2023
Days to Decision
268 days
Submission Type
Summary