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 ...
After receiving 510(k) clearance from the U.S. Food and Drug Administration for its professional defibrillator, the Tempus LS-Manual, Philips today launched its remote-monitoring and defibrillator ...
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