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U.S. Department of Health and Human Services

510(K) Premarket Notification
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31 to 40 of 493 Results
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Device Name
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510(K)
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Decision
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ultra v therapeutic ultrasound EXCEL TECH. LTD. k001166 07/07/2000
ultra compact wrist blood pressure monitor with intellisense, model hem-630 OMRON HEALTHCARE, INC. k001671 06/30/2000
ultra care 2 latex examination gloves made from allotex (enzyme treated) natural rubber latex with a protein content lab TILLOTSON HEALTHCARE CORP. k002718 05/01/2001
u2 hip stem, ti porous coated UNITED ORTHOPEDIC CORP. k003237 01/10/2001
trojan latex condom with male genital desensitizer lubricant ARMKEL, LLC. k000748 04/06/2000
trojan extra large latex condom ARMKEL, LLC. k001212 05/09/2000
trochanteric reattachment device (standard) and (long), model 501-066, 501-067 PIONEER SURGICAL TECHNOLOGY k001709 08/31/2000
trifix spinal fixation system ENDIUS, INC. k001627 06/03/2000
tri-fix spinal fixation system ENDIUS, INC. k000766 06/01/2000
treatvision VARIAN MEDICAL SYSTEMS, INC. k002194 08/18/2000

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