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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 FILTER 02/26/2019
CORDIS CASHEL UNKNOWN OPTEASE VENA CAVA FILTER 02/25/2019
CORDIS CASHEL UNKNOWN OPTEASE FILTER 02/21/2019
CORDIS CASHEL 466P306X 02/19/2019
CORDIS CASHEL UNKNOWN VENA CAVA FILTER 02/15/2019
CORDIS CASHEL UNKNOWN VENA CAVA FILTER 02/14/2019
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 02/08/2019
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 02/06/2019
CORDIS CASHEL UNKNOWN OPTEASE VENA CAVA FILTER 01/30/2019
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER 01/30/2019
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