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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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4 records meeting your search criteria returned- Product Code: LKK Product Problem: Failure to Infuse Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
FLOWONIX MEDICAL, INC. PROMETRA II PROGRAMMABLE PUMP 08/02/2021
CODMAN & SHURTLEFF CODMAN 3000 10/20/2020
FLOWONIX MEDICAL, INC. PROMETRA II PROGRAMMABLE PUMP 10/08/2020
FLOWONIX MEDICAL, INC. PROMETRA II PROGRAMMABLE PUMP 09/16/2020
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