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Single-use Balloon Dilatation Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241888
510(k) Type
Traditional
Applicant
Leo Medical Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/20/2024
Days to Decision
175 days
Submission Type
Summary

Single-use Balloon Dilatation Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241888
510(k) Type
Traditional
Applicant
Leo Medical Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/20/2024
Days to Decision
175 days
Submission Type
Summary