# Barco, Inc

FEI: 3004578804
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: BARCO NV (#9031117)

Address: 3059 Premiere Pkwy, Suite 400, DULUTH, GA, US



## Products

Total registered: 1
Top product codes: KQM
Regulation §: 878.4160

Proprietary names: MDSC-8258, MDSC-2226, MDSC-8232, MDSC-2232, AMM215WTTP, AMM215WTD, MDSC-8255, MDSC-2326, MDSC-8358, MDSC-2324

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004578804%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004578804