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U.S. Department of Health and Human Services

510(K) Premarket Notification
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381 to 390 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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renegade hi-flo microcatheter BOSTON SCIENTIFIC CORP. k000177 04/07/2000
mdi scl-70 test MICRO DETECT, INC. k000934 04/07/2000
kfa-63 knee and foot array MRI DEVICES CORP. k000935 04/07/2000
sterltech water purifier STERLTECH, INC. k000941 04/06/2000
acticoat foam dressing WESTAIM BIOMEDICAL, INC. k000051 04/05/2000
insyte catheter, insyte autoguard catheter BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. k000235 04/05/2000
randox calcium RANDOX LABORATORIES, LTD. k000375 04/05/2000
flextime HERAEUS KULZER, INC. k000629 04/05/2000
skylight imaging system ADAC LABORATORIES k000908 04/05/2000
renaflo ii hf 2000 hemofilter MINNTECH CORP. k000028 04/04/2000

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