# HEARTBEAM

FEI: 3035371769
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: HeartBeam (#10092613)

Address: 2118 Walsh Ave Ste 210, Santa Clara, CA, US



## Products

Total registered: 1
Top product codes: MWJ
Regulation §: 870.2800

Proprietary names: HeartBeam AIMIGo System, HeartBeam System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223035371769%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3035371769