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Coronary Dilatation Balloon Catheter (VesPenetrator®), Coronary Dilatation Balloon Catheter (VesTraveler®), Coronary Dilatation Balloon Catheter (VexPander®)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230374
510(k) Type
Traditional
Applicant
Dongguan TT Medical, Inc
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/29/2023
Days to Decision
136 days
Submission Type
Summary

Coronary Dilatation Balloon Catheter (VesPenetrator®), Coronary Dilatation Balloon Catheter (VesTraveler®), Coronary Dilatation Balloon Catheter (VexPander®)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230374
510(k) Type
Traditional
Applicant
Dongguan TT Medical, Inc
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/29/2023
Days to Decision
136 days
Submission Type
Summary