# PHASE DIAGNOSTICS

FEI: 3014022295
Status: Active
Establishment types: Manufacture Device in the United States for Export Only
Owner/operator: PHASE Diagnostics (#10075679)

Address: 10527 Garden Grove Blvd., Garden Grove, CA, US



## Products

Total registered: 1
Top product codes: QKO
Regulation §: —

Proprietary names: INDICAID COVID-19 IgM/IgG Rapid Test

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014022295%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014022295
