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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)
Number
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Decision
Date
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n-600x with spd, oximax n-600x COVIDIEN k083325 03/09/2009
surgybone SILFRADENT S.R.L. k083569 04/01/2009
revolution tx/i digital radiographic table system GE MEDICAL SYSTEMS k992066 08/30/1999
belleglaze KERR DENTAL MATERIALS CENTER k992067 08/27/1999
status stik, accusign stik PRINCETON BIOMEDITECH CORP. k992068 07/06/1999
cook ultra quiet vacuum pump & regulator COOK UROLOGICAL, INC. k992070 10/27/1999
transvaginal ultrasound probe holder device RON-TECH MEDICAL LTD. k992071 08/27/1999
bolus accessory set I-FLOW CORP. k992072 09/15/1999
ax workstation SIEMENS MEDICAL SOLUTIONS USA, INC. k992073 09/09/1999
mpm regenecare wound gel MPM MEDICAL, INC. k992074 12/23/1999

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