Last synced on 17 May 2024 at 11:06 pm

Uresta®

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233548
510(k) Type
Traditional
Applicant
Resilia Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/3/2024
Days to Decision
152 days
Submission Type
Summary

Uresta®

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233548
510(k) Type
Traditional
Applicant
Resilia Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/3/2024
Days to Decision
152 days
Submission Type
Summary