The North American subsidiary of Amsterdam-based Royal Philips reached an agreement on a consent decree with the U.S. Department of Justice, representing the Food and Drug Administration, the company ...
Philips receives 510(k) clearance from the FDA for its professional defibrillator (Tempus LS- Manual), now offering its remote monitor and defibrillator solution (Tempus ALS) to EMS customers in the U ...
OpenMarkets, a collaborative marketplace for capital medical equipment, has announced multiple providers have already taken advantage of its recently launched OpenMarkets MarketBuy for Philips ...
Royal Philips Electronics (NYSE:PHG, AEX:PHI) today announced that several leading-edge U.S. emergency medical service (EMS) organizations have chosen the Philips HeartStart MRx – an advanced, ...
Washington(CBS.MW) -- The Food and Drug Administration Thursday granted market clearance to Philips Medical Systems' HeartStart Home Defibrillator for use without a prescription. The action marks the ...
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