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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
7 records meeting your search criteria returned- Product Code: FMK Product Problem: Use of Device Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
TRIVIDIA HEALTH, INC. LANCETS 04/16/2019
ROCHE DIABETES CARE, INC. SOFTCLIX ® LANCETS 01/13/2017
ABBOTT DIABETES CARE INC. LANCING DEVICE 06/08/2016
BAYER HEALTHCARE LLC MICROLET2 04/29/2015
BAYER MICROLET 2 02/19/2015
BAYER LANCET 02/19/2015
BAYER HEALTHCARE LLC MICROLET 11/24/2014
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