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Acute Coronary Syndrome Event Detector

FDA product code QBI · Class 3 · Unknown

18
Registered devices
58
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-09-01Angel Medical Systems, Inc.Device reaching End of Service prematurely.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.