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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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17 records meeting your search criteria returned- Product Code: KXK Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BARD BRACHYTHERAPY, INC. -1424526 QUICKLINK 02/03/2018
GE HEALTHCARE IODINE (I-125) SEEDS 02/01/2017
GE HEALTHCARE IODINE (I-125) SEEDS 09/28/2016
GE HEALTHCARE IODINE (I-125) SEEDS 09/28/2016
MEDI-PHYSICS, INC., DBA GE HEALTHCARE IODINE (I-125) SEEDS 11/06/2014
GE HEALRTHCARE IODINE (I-125) SEEDS 10/16/2014
ISORAY MEDICAL, INC GLIASITE RADIATION THERAPY SYSTEM (RTS) 03/27/2014
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