# ABK BIOMEDICAL

FEI: 3013505221
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: ABK Biomedical (#10086030)

Address: 155 Chain Lake Drive, Unit 32, Halifax Nova Scotia, B3S 1B3, CA

Mandatory US Agent: ABK Biomedical, Inc

## Products

Total registered: 1
Top product codes: KRD
Regulation §: 870.3300

Proprietary names: Easi-Vue® embolic microspheres System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013505221%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013505221