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U.S. Department of Health and Human Services

510(k) Premarket Notification
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71 to 80 of 167 Results
ProductCode: MNR Decision Date To: 09/26/2021
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510(K)
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vitascore VITASCORE B.V. K072014 11/08/2007
clinical oxygen dose recorder (codr), model 300-cr INSPIRED TECHNOLOGIES, INC. K082853 03/23/2009
galaxy RESPIRONICS INC., SLEEP & HOME RESPIRATORY GROUP K083874 01/26/2009
provent nasal cannula VENTUS MEDICAL, INC. K080983 08/07/2008
rmx physiological data recorder S.L.P. LTD. K080375 09/02/2008
watch-pat model 100s-2 ITAMAR MEDICAL K080427 05/23/2008
watch-pat 200i (wp200i) ITAMAR MEDICAL K081037 06/09/2008
somnowatch SOMNOMEDICS GMBH K081485 09/18/2008
watch-pat 200s-2 (wp200s-2) ITAMAR MEDICAL K081982 08/14/2008
somnolyzer 24x7 THE SIESTA GROUP NORTH AMERICA K083620 03/06/2009
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