Last synced on 2 May 2025 at 11:05 pm

OutFlo Aortic Valve Dilatation Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241562
510(k) Type
Traditional
Applicant
DISA Medinotec
Country
South Africa
FDA Decision
Substantially Equivalent
Decision Date
3/11/2025
Days to Decision
284 days
Submission Type
Summary

OutFlo Aortic Valve Dilatation Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241562
510(k) Type
Traditional
Applicant
DISA Medinotec
Country
South Africa
FDA Decision
Substantially Equivalent
Decision Date
3/11/2025
Days to Decision
284 days
Submission Type
Summary