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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
CORDIS US CORP. SABERX RADIANZ PTA DILATION CATHERE 12/30/2022
CORDIS US CORP. SABERX RADIANZ PTA DILATION CATHERE 12/30/2022
CORDIS CORPORATION SABER RX 6MM6CM 155 12/30/2022
CORDIS US. CORP MAXI LD PTA F7 110 14X6 12/30/2022
CORDIS US. CORP 4 FR SABERX RADIANZ 4MM8CM 190 12/30/2022
CORDIS US. CORP 4FR SABERX RADIANZ 5MM10CM 190 12/30/2022
CORDIS US. CORP 4FR SABERX RADIANZ 5MM10CM 190 12/30/2022
CORDIS CORPORATION SABER RX 3MM10CM 155 12/30/2022
BARD PERIPHERAL VASCULAR, INC. ULTRAVERSE 035 12/30/2022
CORDIS CORPORATION SABER RX 3MM30CM 155 12/29/2022
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