About this listing
KardiaAI from AliveCor, Inc. appears on the U.S. FDA list of AI-enabled medical devices under submission K201985. It went through the 510(k) pathway, reviewed by the Cardiovascular panel, with an FDA decision dated November 12, 2020. Its primary FDA product code is DQK.
The FDA list records the regulatory facts above. For the device's cleared intended use, read the FDA decision summary linked at the bottom of this page.
- Device
- KardiaAI
- Company
- AliveCor, Inc.
- Submission number
- K201985
- Pathway
- 510(k)
- Decision date
- Nov 12, 2020
- Specialty (lead panel)
- Cardiovascular
- Primary product code
- DQK
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Source: U.S. FDA AI-Enabled Medical Devices list. The FDA says the list is not comprehensive. Confirm details on the FDA's own record.