510(k) DEN180042 ยท QDB Photoplethysmograph Analysis Software For Over-The-Counter Use
Irregular Rhythm Notification Feature
| Applicant | Apple, Inc., Alexandria VA, US |
| Decision | Unknown, Sep 11, 2018 |
| Received | Aug 9, 2018 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN180042
No recall in the FDA data names this 510(k).
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