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U.S. Department of Health and Human Services

510(K) Premarket Notification

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161 to 170 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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flexi-site sp02 ear sensor EPIC MEDICAL EQUIPMENT SERVICES, INC. k010718 03/23/2001
fluoroplastic ventilation tubes GYRUS ENT L.L.C. k992222 08/26/1999
fountain infusion catheter and occluding guide wire MERIT MEDICAL SYSTEMS, INC. k992231 07/23/1999
fresenius modified f400 low volume hemoconcentrator f3000 & modified f400 low vol hemoconcentrator w/tubing set f3000ts FRESENIUS USA, INC. k992275 08/04/1999
frolov's respiration training device, frtd-01 INTERCONTINENTAL NEW TECHNOLOGIES, INC. k992256 01/11/2000
fusion fast GC AMERICA, INC. k043471 01/27/2005
future mobility healthcare inc. orion ii wheelchair and stellato mechanical wheelchair FUTURE MOBILITY HEALTHCARE INC. k061010 05/23/2006
ge logiq 200 md diagnostic ultrasound system GE MEDICAL SYSTEMS, INC. k992208 07/12/1999
ge logiq works GENERAL ELECTRIC CO. k063006 11/02/2006
geiger electrosurgical handpiece sheath, model 405 GEIGER MEDICAL TECHNOLOGIES, INC. k992149 08/19/1999

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