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U.S. Department of Health and Human Services

510(K) Premarket Notification
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171 to 180 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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pc coated fluoroplastic vent tubes GYRUS ENT L.L.C. k000801 06/19/2000
pbn fallopian tube catheter system MEDICAL DEVICE TECHNOLOGIES, INC. k000620 10/30/2000
pathway cts 2000 pelvic floor training system, model pathway cts 2000 THE PROMETHEUS GROUP k001515 07/31/2000
pass spinal system ENCORE ORTHOPEDICS, INC. k001024 05/23/2000
pasco mic and mic/id panels PASCO LABORATORIES, INC. k001516 07/12/2000
parietex composite (pco) mesh MEDICAL DEVICE CONSULTANTS, INC. k002699 02/15/2001
otw megalink sds biliary stent system ADVANCED CARDIOVASCULAR SYSTEMS, INC. k000550 03/17/2000
oti ceramic femoral head system OSTEOIMPLANT TECHNOLOGY, INC. k003316 01/19/2001
os-2000 optical sonography system ADVANCED DIAGNOSTICS, INC. k001510 11/30/2000
orthone ONI, INC. k001773 08/18/2000

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