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U.S. Department of Health and Human Services

510(K) Premarket Notification
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191 to 200 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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hitachi airis ii HITACHI MEDICAL SYSTEMS AMERICA, INC. k001334 07/06/2000
hoffmann ii dynamization/distraction rod-to-rod coupling HOWMEDICA OSTEONICS CORP. k003211 12/15/2000
hydro-cast bis-acryl temporary crown and bridge material, model 98250 KAY SEE DENTAL MFG. CO. k001309 06/13/2000
hystalog hsg catheter ROCKET MEDICAL PLC k000340 04/19/2000
ics medical chartr ep and chartr oae systems ICS MEDICAL CORP. k002985 12/13/2000
ifa kit for the detection of endomysial iga anibodies using primate umbilical cord (puc)-ema/puc lga. SCIMEDX CORP. k002107 08/04/2000
image x-70 plus dental x-ray unit MEDICAL DEVICE CONSULTANTS, INC. k000551 03/16/2000
impact modular total hip system BIOMET, INC. k000334 02/16/2000
impulse select AIRSEP CORP. k001579 08/31/2000
incentive spirometer ENGINEERED MEDICAL SYSTEMS k000314 04/12/2000

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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