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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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6 records meeting your search criteria returned- Product Code: DTK Product Problem: Cannula Guide Report Date From: 01/1/2014
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ManufacturerBrand NameDate Report Received
CORDIS CORPORATION OPTEASE RETR FILTER 55 03/30/2020
CORDIS CASHEL OPTEASE RETR FILTER 55 11/20/2019
CORDIS CASHEL OPTEASE RETR FILTER 55 FEMORAL 04/03/2018
CORDIS CASHEL FEMORAL 55CM KIT 10/09/2017
CORDIS CASHEL FEMORAL 55CM KIT 10/09/2017
CORDIS CASHEL OPTEASE RETR FILTER 55 FEMORAL 09/25/2017
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