Atrial Fibrillation History Feature— 510(k) K213971
Substantially EquivalentApple, Inc.
FDA 510(k) clearance K213971 for Atrial Fibrillation History Feature, Substantially Equivalent on 2022-06-03. Applicant: Apple, Inc.. Device class: 2.
Clearance details
- Applicant
- Apple, Inc.
- Product code
- Code QDB
- Device class
- Class 2
- Regulation
- 21 CFR 870.2790
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cupertino, CA, US
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