SHENZHEN, China, March 31, 2008 /Xinhua-PRNewswire via COMTEX News Network/ -- Mindray Medical International Limited (NYSE: MR) today announced it has received 510(k) clearance from the United States Food and Drug Administration ("FDA") for its portable M5 ultrasound imaging system and BS-200 automatic bio-chemistry analyzer. Mindray has to date received FDA 510(k) clearance for a total of 14 products, covering patient monitoring and life support products, in-vitro diagnostic products and medical imaging systems.
The company also announced it has received approval from the Chinese State Food and Drug Administration ("SFDA") for the M5 and its DC-3 color ultrasound imaging system and provided an update on its product approval pipeline.
source: Mindray
Wednesday, April 2, 2008
Mindray's Laptop-size M5 and BS-200 Receive FDA Clearance
at 4:20 PM
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