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U.S. Department of Health and Human Services

510(K) Premarket Notification
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51 to 60 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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autovac orthopedic autotransfusion system BOEHRINGER LABORATORIES k014187 02/06/2002
axiamed trans-sacral spinal access device AXIAMED, INC. k020457 09/26/2002
baby face SONORA MEDICAL SYSTEMS k994385 03/16/2000
bactec mgit 960 sire kits BECTON, DICKINSON & CO. k014123 04/19/2002
bacti-swab dry REMEL CO. k013711 11/26/2001
ballpen spinal needle w/wo introducer RUSCH INTL. k011122 11/16/2001
bard utaverse small vessel pta balloon dilatation catheter C.R. BARD, INC. k012913 09/28/2001
bardport x-port isp port C.R. BARD, INC. k022983 09/25/2002
bd phoenix automated microbiology system BECTON, DICKINSON & CO. k023568 01/24/2003
bd phoenix automated microbiology system - gentamicin 0.25 - 16 ug/ml BECTON, DICKINSON & CO. k023273 10/31/2002

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