KardiaMobile 6L— 510(k) K220350

Substantially Equivalent

AliveCor, Inc.

FDA 510(k) clearance K220350 for KardiaMobile 6L, Substantially Equivalent on 2022-05-25. Applicant: AliveCor, Inc..

Clearance details

Applicant: AliveCor, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 2022-02-07
Decision date: 2022-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

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