# CLEARFLOW, INC

FEI: 3008782989
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: ClearFlow, Inc. (#10034650)

Address: 16 Technology Drive. Suite 150, Irvine, CA, US



## Products

Total registered: 2
Top product codes: OTK, GBX
Regulation §: 878.4780, 878.4200

Proprietary names: PleuraFlow System with FlowGlide 20FR SEDL, PF-20 SEDL

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008782989%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008782989