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VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video Box

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223926
510(k) Type
Traditional
Applicant
Medimaging Integrated Solution Inc. (MiiS)
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/6/2023
Days to Decision
280 days
Submission Type
Summary

VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video Box

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223926
510(k) Type
Traditional
Applicant
Medimaging Integrated Solution Inc. (MiiS)
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/6/2023
Days to Decision
280 days
Submission Type
Summary