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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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3 records meeting your search criteria returned- Product Code: KXG Product Problem: Labelling, Instructions for Use or Training Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
CAREFUSION 213, LLC 0113 UNKNOWN CHLORAPREP 04/20/2021
CAREFUSION 213, LLC 0113 CHLORAPREP SWABSTICK 04/07/2021
CAREFUSION, INC CHLORAPREP ONE-STEP HI-LITE ORANGE 01/14/2021
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