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U.S. Department of Health and Human Services

510(K) Premarket Notification
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Device Name
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510(K)
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salute ii disposable fixation device, models 0113070, 0113072, 0113073, 0113077, 0113079 DAVOL INC., SUB. C.R. BARD, INC. k051848 08/11/2005
vitek 2 gram positive ertapenem for streptococcus pneumoniae BIOMERIEUX, INC. k051849 08/16/2005
aviso ophthalmic ultrasound system QUANTEL MEDICAL k051851 08/03/2005
single amplifier for botox ALLERGAN, INC. k051852 09/14/2005
cardiostream sonoaim CARDIOSTREAM, LLC k051853 08/22/2005
clever chek td-4225, model td-4225 TaiDoc Technology Corporation k051854 08/05/2005
ventri GE MEDICAL SYSTEMS F.I. HAIFA k051855 08/02/2005
trans1 facet screws TRANS1 INCORPORATED k051856 09/26/2005
veo multigas monitor for pocket pc, model 400221 WEISSBURG ASSOCIATES k051857 09/15/2005
acumatch m-series lpb 12/14 femoral stem EXACTECH, INC. k051858 12/01/2005

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