Home » CAS ANNOUNCES FDA 510(K) CLEARANCE FOR EXPANDED USE OF FORE-SIGHT(TM) CEREBRAL OXIMETER
CAS ANNOUNCES FDA 510(K) CLEARANCE FOR EXPANDED USE OF FORE-SIGHT(TM) CEREBRAL OXIMETER
CAS Medical Systems announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for expanded use of its FORE-SIGHT Absolute Cerebral Oximeter in additional patient populations including children over 40 kg and infants.
CASMed
KEYWORDS FDAnews Device Daily Bulletin
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