Philips recently announced that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a ...
SILVER SPRING, Md. — The Food and Drug Administration on Tuesday issued a safety communication on HeartStart automated external defibrillators from Philips Healthcare, noting that certain HeartStart ...
Royal Philips Electronics (NYSE: PHG, AEX: PHI) is introducing Philips HeartStart FR3 automated external defibrillator (AED) during Arab Health, for professional responders in the region who treat ...
Clever design, close attention to human safety issues, and a top man-machine interface make the Philips HeartStart portable home defibrillator one of the hottest medical electronics devices on the ...
Amsterdam, the Netherlands and Cambridge, MA– Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the Center for Devices and Radiological Health (CDRH) ...
The US Food and Drug Administration (FDA) is classifying a recent safety notice covering certain models of the HeartStart MRx Monitor/Defibrillator due to electrical and battery connection issues as a ...
According to a press release from the FDA, certain HeartStart automated external defibrillators (AEDs) may not be able to deliver the necessary shock in a cardiac emergency. The FDA released this ...
U.S. patent number 6,871,093 B2, assigned to Koninklijke Philips Electronics N.V., Eindhoven, the Netherlands and listing the inventor as Kim J. Hansen, Renton, Wash., describes the earliest details ...
Please provide your email address to receive an email when new articles are posted on . The FDA has issued a safety communication indicating that certain HeartStart automated external defibrillators ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results