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Ureterorenoscope System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240374
510(k) Type
Traditional
Applicant
Shenzhen HugeMed Medical Technical Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/10/2024
Days to Decision
93 days
Submission Type
Summary

Ureterorenoscope System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240374
510(k) Type
Traditional
Applicant
Shenzhen HugeMed Medical Technical Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/10/2024
Days to Decision
93 days
Submission Type
Summary