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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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 SKYPOINT DRUG ELUTING CORONARY ST 09/17/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY XD 09/08/2021
MEDTRONIC IRELAND RESOLUTE ONYX RX 09/02/2021
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 06/28/2021
MEDTRONIC IRELAND RESOLUTE ONYX RX 06/22/2021
ABBOTT VASCULAR XIENCE PRIME SV EVEROLIMUS ELUTING CORON 06/16/2021
MEDTRONIC IRELAND RESOLUTE ONYX RX 06/14/2021
MEDTRONIC IRELAND RESOLUTE ONYX RX 06/09/2021
MEDTRONIC IRELAND RESOLUTE ONYX RX 05/31/2021
MEDTRONIC IRELAND RESOLUTE ONYX OTW 05/07/2021
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