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Arise™ UHP Dilatation Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230191
510(k) Type
Traditional
Applicant
Creagh Medical Ltd
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/22/2023
Days to Decision
57 days
Submission Type
Summary

Arise™ UHP Dilatation Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230191
510(k) Type
Traditional
Applicant
Creagh Medical Ltd
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/22/2023
Days to Decision
57 days
Submission Type
Summary