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U.S. Department of Health and Human Services

510(K) Premarket Notification
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351 to 360 of 500 Results *
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Device Name
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Applicant
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510(K)
Number
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Decision
Date
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vapotherm, model 2000i VAPOTHERM, INC. k000401 08/24/2000
odontosurge 3 ODONTO-WAVE k001560 08/24/2000
plainsense wheelchair PLAINSENSE WHEELCHAIRS, INC. k001909 08/25/2000
regency power wheelchair, model 7200, 7500 & 7800 GENDRON, INC. k001923 08/25/2000
spina system NORTH AMERICAN MEDICAL CORPORATION (NAM) k002260 08/25/2000
improved try-in gel SYBRON DENTAL SPECIALTIES, INC. k001899 08/28/2000
neocontrol pelvic floor therapy system NEOTONUS, INC. k001903 08/29/2000
depuy neuflex pip finger DEPUY, INC. k001922 08/29/2000
128 channel eeg headbox, model ex-nw-128 EXCEL TECH. LTD. k000919 08/31/2000
vasotrax MEDWAVE, INC. k001898 08/31/2000

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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