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Vericor Support Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222679
510(k) Type
Traditional
Applicant
VascuPatent Medical (Shenzhen) Co. Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/7/2022
Days to Decision
62 days
Submission Type
Summary

Vericor Support Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222679
510(k) Type
Traditional
Applicant
VascuPatent Medical (Shenzhen) Co. Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/7/2022
Days to Decision
62 days
Submission Type
Summary