# MIRAVISTA DIAGNOSTICS

FEI: 3005369540
Status: Active
Establishment types: Manufacture Device in the United States for Export Only
Owner/operator: MiraVista Diagnostics (#10077725)

Address: 4705 Decatur Boulevard, Indianapolis, IN, US



## Products

Total registered: 1
Top product codes: MIZ
Regulation §: 866.3320

Proprietary names: Histoplasma urine antigen control kit, Histoplasma urine antigen LFA test kit

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005369540%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005369540