KardiaMobile 6L— 510(k) K210753
Substantially EquivalentAliveCor, Inc.
FDA 510(k) clearance K210753 for KardiaMobile 6L, Substantially Equivalent on 2021-06-30. Applicant: AliveCor, Inc.. Device class: 2.
Clearance details
- Applicant
- AliveCor, Inc.
- Product code
- Code DXH
- Device class
- Class 2
- Regulation
- 21 CFR 870.2920
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountain View, CA, US
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