FDA 510(k) Applications for Medical Device Product Code "NMD"
(Oximeter, Tissue Saturation, Reprocessed)

FDA 510(k) Number Applicant Device Name Decision Date
K100523 HYGIA HEALTH SERVICES, INC. ADULT CEREBRAL-SOMATIC OXIMETRY SENSOR, PEDIATRIC CEREBRAL-SOMATIC OXIMETRY SENSOR MODEL HHS-SAFB-SM, HHS-SPFB-USA 05/04/2010
K111007 MIDWEST REPROCESSING CENTER LLC MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE 06/08/2011


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