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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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pjur eros water formulation L.C.C. PJUR GROUP GERMANY k010199 04/05/2001
piper RTEK MEDICAL SYSTEMS, LLC. k001295 10/25/2000
permlastic 3 SYBRON DENTAL SPECIALTIES, INC. k003650 02/15/2001
perclose vascular suture delivery device ABBOTT VASCULAR INC. k001703 10/03/2000
pelvic muscle therapy COLONIAL MEDICAL SUPPLY k002830 12/27/2000
pectofix dynamic sternal fixation system (dsf) PECTOFIX, INC. k000694 05/11/2000
pe.r.i. ii knee fracture system DEPUY ORTHOPAEDICS, INC. k003235 11/06/2000
pbn hystero-salpingography catheter set MEDICAL DEVICE TECHNOLOGIES, INC. k000433 06/16/2000
paragon cze 2000 capillary electrophoresis system and buffer-100 BECKMAN COULTER, INC. k002799 10/05/2000
pain care multi-port catheter, model 2000l BREG, INC. k003611 12/13/2000

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