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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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7 records meeting your search criteria returned- Product Code: FMF Patient Problem: Not Applicable Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 04/20/2017
COVIDIEN MONOJECT 03/06/2017
COVIDIEN LP/LLC, NORFOLK MONOJECT 02/22/2017
COVIDIEN MONOJECT 02/21/2017
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN 3 02/16/2017
COVIDIEN MONOJECT 02/16/2017
NOVO NORDISK A/S NOVOPEN 4 12/07/2015
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