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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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11 records meeting your search criteria returned- Product Code: NIQ Product Problem: Unintended System Motion Report Date From: 01/1/2015
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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE SIERRA 09/16/2019
ABBOTT VASCULAR XIENCE SIERRA 07/24/2019
AV-TEMECULA-CT XIENCE XPEDITION EVEROLIMUS ELUTING CORO 12/21/2018
AV-TEMECULA-CT XIENCE XPEDITION EVEROLIMUS ELUTING CORO 12/17/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 11/15/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/31/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/31/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/28/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/24/2018
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 08/22/2018
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