FDA Device Intelligence
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Aid, Cardiopulmonary Resuscitation

FDA product code LIX · Class 2 · Cardiovascular

35
Registered devices
153
Adverse events
2
Recalls
17
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-01-29Philips Electronics North America CorporationInform users of correct placement of the disposable adhesive pad on the QCPR meter and inform users of injuries associated with proper performance of CPR. As
2018-01-29Philips Electronics North America CorporationInform users of correct placement of the disposable adhesive pad on the QCPR meter and inform users of injuries associated with proper performance of CPR. As

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