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Philips Receives FDA 510(k) Clearance for Its Most Advanced Acute Patient Monitors

Philips Receives FDA 510(k) Clearance for Its Most Advanced Acute Patient Monitors

Amsterdam, the Netherlands, Dec. 8 (Korea Bizwire) – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that its Philips Patient Monitors MX750 and MX850 have received 510(k) clearance from the U.S. Food and Drug Administration. Initially cleared for Emergency Use Authorization in 2020, the MX750 and MX850 are Philips’ most advanced patient monitors uniquely designed to support [...]