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Over-The-Counter Automated External Defibrillator

FDA product code NSA · Class 3 · Cardiovascular

5
Registered devices
1,801
Adverse events
2
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2009-11-02Philips Medical SystemsPotential for failure of a capacitor during use which would prevent the AED from delivering effective defibrillation therapy when indicated.
2008-04-30Philips Medical SystemsButtons Sticking - The On/Off and Shock buttons on the front panel of the device may stick in place when pressed and fail to respond to the button press, causin

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