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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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510(K)
Number
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Decision
Date
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ascent knee revision femoral stem Biomet, Inc. k001010 04/27/2000
elecsys thyroglobulin calcheck Roche Diagnostics Corp. k001015 04/27/2000
ti500 globe-trotter transport system Hill-Rom Air-Shields k001019 04/27/2000
lilliput phospholypidic inert surface in oxygenation (ph.i.s.i.o.) infant hollow fibre oxygenator, model d902 Dideco S.P.A. k001021 04/25/2000
evershears bipolar scissors Everest Medical Corp. k000496 04/24/2000
matang powdered latex patient examination glove with protein labeling claim (50 microgram or less Matang Mfg. Sdn. Bhd. k000985 04/24/2000
ge logiq 700 GE Medical Systems k001016 04/24/2000
cavermap surgical aid Uromed Corp. k000507 04/21/2000
view nt Electromed Intl., Ltd. k000474 04/19/2000
the cyberknife system for stereotactic radiosurgery/ radiotherapy v2.1 Accuray, Inc. k000478 04/19/2000

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