VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video Box— 510(k) K223926
Substantially EquivalentMedimaging Integrated Solution, Inc (Miis)
FDA 510(k) clearance K223926 for VersaVue Single-Use Flexible Cystoscope, VersaVue Tablet, and VersaVue Video Box, Substantially Equivalent on 2023-10-06. Applicant: Medimaging Integrated Solution, Inc (Miis).
Clearance details
- Applicant
- Medimaging Integrated Solution, Inc (Miis)
- Product code
- Code FAJ
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hsinchu, CN
Adverse events under product code FAJ
product code FAJ- Injury
- 533
- Malfunction
- 6,705
- Total
- 7,238
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.