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U.S. Department of Health and Human Services

510(K) Premarket Notification

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151 to 160 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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aems v, ems-1000, model ts-140500 and aems vi, ems-1000 plus, model ts-140600 Apex Medical Corp. k002339 08/24/2001
ksea dion-gracia set KARL STORZ Endoscopy-America, Inc. k010785 08/21/2001
aia-pack brca, st aia pack brca Tosoh Medics, Inc. k010796 08/16/2001
ms104a, newmini ii (ems-ii), model ap-101050t and medtrim (ems-v), model ap-102050t Apex Medical Corp. k002336 07/27/2001
tacker, model r65-933 A & A Medical, Inc. k003949 07/25/2001
wundcath conduction catheter Micor, Inc. k003966 07/17/2001
stimulan - calcium sulfate bone void filler kit Biocomposites, Ltd. k003954 07/12/2001
trochanteric nail DePuy Orthopaedics, Inc. k010780 06/12/2001
sigma delta Penlon , Ltd. k002343 06/08/2001
remote presence and care system (rpcs 5000) Adsis , Ltd. k010791 06/08/2001

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