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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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229 records meeting your search criteria returned- Product Code: KFM Product Problem: Insufficient Information Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 01/23/2023
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 01/23/2023
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 01/18/2023
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, OUS 01/13/2023
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 12/20/2022
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, OUS 12/19/2022
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 12/13/2022
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 11/30/2022
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, US 11/29/2022
THORATEC SWITZERLAND GMBH CENTRIMAG MOTOR, OUS 11/22/2022
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