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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE XPEDITION 48 EVEROLIMUS ELUTING C 09/23/2020
ABBOTT VASCULAR XIENCE V EVEROLIMUS ELUTING CORONARY STE 09/23/2020
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 09/22/2020
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 09/21/2020
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 09/21/2020
ABBOTT VASCULAR XIENCE SIERRA 09/21/2020
ABBOTT VASCULAR XIENCE PRIME LL EVEROLIMUS ELUTING CORON 09/16/2020
ABBOTT VASCULAR XIENCE PRIME LL EVEROLIMUS ELUTING CORON 09/16/2020
ABBOTT VASCULAR XIENCE PRIME EVEROLIMUS ELUTING CORONARY 09/16/2020
ABBOTT VASCULAR XIENCE PRIME EVEROLIMUS ELUTING CORONARY 09/15/2020
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