# Bistos co., ltd.

FEI: 3006179052
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Bistos Co., Ltd. (#10023402)

Address: 522, Geumeo-ro, Pogok-eup,, Cheoin-gu,, Yongin-si Gyeonggi, 17030, KR

Mandatory US Agent: Bistos America

## Products

Total registered: 1
Top product codes: HGM
Regulation §: 884.2740

Proprietary names: Fetal Doppler, Hi-bebe, BT-200T

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006179052%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006179052