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U.S. Department of Health and Human Services

510(K) Premarket Notification

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171 to 180 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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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
funnel trocar PATTON MEDICAL CORP. k992324 08/19/1999
fuzzy automatic blood pressure monitor models md-750, md-770, md-800 MEDITEC CO., LTD. k992328 07/21/1999
gallini biosystem bone marrow aspiration/biopsy needle GALLINI U.S., LLC. k992499 08/12/1999
ge logiq 200 md diagnostic ultrasound system GE MEDICAL SYSTEMS, INC. k992208 07/12/1999
geiger electrosurgical handpiece sheath, model 405 GEIGER MEDICAL TECHNOLOGIES, INC. k992149 08/19/1999
gendex 765dc, model 110-0154 DENTSPLY INTL. k992610 09/07/1999
general purpose transducer standoff, biopsy transducer standoff, bi-plane endocavity transducer standoff CIVCO MEDICAL INSTRUMENTS CO., INC. k992152 08/17/1999

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