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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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Applicant
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510(K)
Number
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Decision
Date
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hoffman hoop device Howmedica Corp. k810644 03/24/1981
histogrip & histogrip gold concentrate/prediluted Stat Path k881477 04/18/1988
histofreezer Solarcare Technologies Corp,Inc. k931299 08/11/1993
hill tube Physio-Control Corp. k771723 11/22/1977
hi vision preirus doagnostic ultrasound scanner model hi vision preirus Hitachi Medical Systems America, Inc. k093466 06/17/2010
hgb-cal set/multiple R&D Systems, Inc. k893984 08/15/1989
hewlett-packard models m1400a, m1402a & m1401a Hewlett-Packard Co. k911139 06/11/1991
herbert bone screw Zimmer, Inc. k792022 10/26/1979
hemoglide series and hemoglide star series xk long-term hemodialysis catheters C.R. Bard, Inc. k051748 08/12/2005
hematrak maturity profile option Geometric Data, Div. Smithkline Corp. k761208 02/28/1977

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