Last synced on 24 May 2024 at 11:04 pm

2-Way 100% Silicone Cleartract Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233013
510(k) Type
Traditional
Applicant
Silq Technologies Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2024
Days to Decision
123 days
Submission Type
Summary

2-Way 100% Silicone Cleartract Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233013
510(k) Type
Traditional
Applicant
Silq Technologies Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2024
Days to Decision
123 days
Submission Type
Summary