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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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269 records meeting your search criteria returned- Product Code: DTK Patient Problem: Embolus Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER 11/27/2018
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55 CMCSI 11/27/2018
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER 11/26/2018
CORDIS CASHEL JUGULAR 55CM KIT 11/26/2018
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER 11/26/2018
CORDIS CASHEL UNKNOWN OPTEASE VENA CAVA FILTER 11/20/2018
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER 11/20/2018
CORDIS CASHEL UNKNOWN OPTEASE VENA CAVA FILTER 11/20/2018
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 11/16/2018
CORDIS CASHEL 466FXXXX 11/13/2018
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