Last synced on 14 November 2025 at 11:06 pm

KardiaMobile, KardiaStation

Page Type
Cleared 510(K)
510(k) Number
K182396
510(k) Type
Traditional
Applicant
AliveCor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2019
Days to Decision
220 days
Submission Type
Summary

KardiaMobile, KardiaStation

Page Type
Cleared 510(K)
510(k) Number
K182396
510(k) Type
Traditional
Applicant
AliveCor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2019
Days to Decision
220 days
Submission Type
Summary