Last synced on 14 November 2025 at 11:06 pm

Seclusion Catheter

Page Type
Cleared 510(K)
510(k) Number
K243436
510(k) Type
Traditional
Applicant
Basis Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
115 days
Submission Type
Summary

Seclusion Catheter

Page Type
Cleared 510(K)
510(k) Number
K243436
510(k) Type
Traditional
Applicant
Basis Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2025
Days to Decision
115 days
Submission Type
Summary