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U.S. Department of Health and Human Services

510(K) Premarket Notification

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71 to 80 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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smith & nephew suture anchor SMITH & NEPHEW, INC. k003599 02/15/2001
conductive gel for ultrasound SKYLARK DEVICE & SYSTEMS CO., LTD k002832 08/06/2001
heliodent vario SIRONA DENTAL SYSTEMS GMBH k000672 05/02/2000
cpap system, model 102001 SIMS PORTEX, INC. k001318 07/20/2000
siemens infinity modular monitors model sc 8000; sc 7000; sc 9000xl SIEMENS MEDICAL SOLUTIONS USA, INC. k003243 12/21/2000
siemens multi view workstation with vent viewer option SIEMENS MEDICAL SOLUTIONS USA, INC. k003246 12/21/2000
interactive real time scanning package SIEMENS MEDICAL SOLUTIONS USA, INC. k003623 12/21/2000
magnetom rhapsody system SIEMENS MEDICAL SOLUTIONS USA, INC. k003628 01/23/2001
modification to kion anesthesia system SIEMENS ELEMA AB k001315 05/26/2000
nirtrile patient examination glove (blue color) powdered, non sterile SIAM SEMPERMED CORP. LTD. k002818 11/29/2000

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