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U.S. Department of Health and Human Services

510(k) Premarket Notification

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51 to 60 of 500 Results *
Decision Date To: 07/22/2019
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510(K)
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beddr 200 system Hancock Medical, Inc. K190399 08/05/2019
fluorospeed Shimadzu Corporation K191877 08/05/2019
046 zenith flex InNeuroCo, Inc K190338 08/02/2019
epicardial access system Baylis Medical Company Inc. K191546 08/02/2019
advia centaur erythropoietin (epo) assay Axis-Shield Diagnostics Limited K183088 08/02/2019
hamilton-t1, hamilton-c1 Hamilton Medical AG K181216 08/02/2019
apa oxy blade Venner Medical (Singapore) Pte Ltd K191602 08/02/2019
dynosense vital sign measuring system DynoSense Corp. K190090 08/02/2019
mobilediagnost wdr 2.2 Sedecal SA K191813 08/02/2019
single use cytology brush bc-205d Olympus Medical Systems Corp. K190293 08/02/2019

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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