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Ureteral Stents (AF-D series)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243039
510(k) Type
Traditional
Applicant
Alton (Shanghai) Medical Instruments Co. Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/18/2025
Days to Decision
264 days
Submission Type
Summary

Ureteral Stents (AF-D series)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243039
510(k) Type
Traditional
Applicant
Alton (Shanghai) Medical Instruments Co. Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/18/2025
Days to Decision
264 days
Submission Type
Summary