VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT— 510(k) K011031
Substantially EquivalentVysis
FDA 510(k) clearance K011031 for VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT, Substantially Equivalent on 2001-08-03. Applicant: Vysis.
Clearance details
- Applicant
- Vysis
- Product code
- Code MMW
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Downers Grove, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.