Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name computer, diagnostic, programmable
510(k) Number K181823
Device Name KardiaAI
Applicant
AliveCor, Inc.
444 Castro Street, Suite 600
Mountain View,  CA  94041
Applicant Contact Prabhu Raghavan
Correspondent
AliveCor, Inc.
444 Castro Street, Suite 600
Mountain View,  CA  94041
Correspondent Contact Prabhu Raghavan
Regulation Number870.1425
Classification Product Code
DQK  
Subsequent Product Code
DPS  
Date Received07/09/2018
Decision Date 03/11/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-