Last synced on 6 December 2024 at 11:05 pm

SmartGUIDE deflectable hydrophilic guidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222690
510(k) Type
Traditional
Applicant
Artiria Medical SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/24/2023
Days to Decision
230 days
Submission Type
Summary

SmartGUIDE deflectable hydrophilic guidewire

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222690
510(k) Type
Traditional
Applicant
Artiria Medical SA
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/24/2023
Days to Decision
230 days
Submission Type
Summary