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U.S. Department of Health and Human Services

510(K) Premarket Notification

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181 to 190 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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polyurethane blood pressure cuffs D. E. HOKANSON, INC. k041689 08/06/2004
i3 system-abd diagnostic ultrasound INNOVATIVE IMAGING, INC. k041947 08/16/2004
flowmedic, model 220 FLOWMEDIC (ISRAEL) LTD k042217 01/12/2005
procedur 10 syringe device AVANCA MEDICAL DEVICES, INC. k042486 01/21/2005
camino slim-line intracranial monitoring system NOVUS MONITORING LTD k042728 10/22/2004
i open 0.36 t-magnetic resonance imaging system WANDONG MEDICAL k042948 11/03/2004
vertebron pss pedicle screw system VERTEBRON, INC. k043152 02/01/2005
open radiotransparent intersomatic implant (roi) LDR SPINE USA k043349 06/29/2005
cryocheck clot s PRECISION BIOLOGIC INC. k043571 03/18/2005
langston dual lumen pressure monitoring catheter VASCULAR SOLUTIONS, INC. k050168 05/18/2005

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