# AliveCor

FEI: 3009715978
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: AliveCor, Inc. (#10041430)

Address: 189 N Bernardo Avenue, Suite 100, Mountain View, CA, US



## Products

Total registered: 3
Top product codes: QDA, DXH, DPS
Regulation §: 870.2345, 870.2920, 870.2340

Proprietary names: Kardia 6L+, KardiaMobile 6L Max, KARDIAMOBILE 6L, K1000

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009715978%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009715978