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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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Decision
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macroporepx pediatric system MACROPORE BIOSURGERY, INC. k002207 07/11/2001
magna 5000 phased array ctl spine coil USA INSTRUMENTS, INC. k000002 02/23/2000
magnetom allegra system SIEMENS MEDICAL SOLUTIONS USA, INC. k002179 10/11/2000
mallory head modular calcar BIOMET ORTHOPEDICS, INC. k001660 06/14/2000
medica hp 300 hemofiltration pump, model 300 MEDICA S.R.L. k000724 03/22/2001
medline blockade or resistat surgical gowns and surggical drapes MEDLINE INDUSTRIES, INC. k003755 02/16/2001
medtronic ave bridge x3 stent MEDTRONIC AVE, INC. k000744 06/05/2000
medtronic dlp arterial cannulae with 3d tip MEDTRONIC CARDIAC SURGICAL PRODUCTS k000776 02/07/2001
medtronic solan fiberoptic corneal light probe MEDTRONIC XOMED k000728 03/21/2000
memcath urology introducer sheath, model 201 MEMCATH TECHNOLOGIES LLC. k000767 06/05/2000

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