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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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
 

 
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111 records meeting your search criteria returned- Product Code: CGA Product Problem: Low Test Results Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ARKRAY, INC. RELION PRIME BLOOD GLUCOSE SYSTEM 07/08/2014
NIPRO DIAGNOSTICS, INC. TRUETRACK 07/03/2014
SIEMENS HEALTHCARE DIAGNOSTICS DIMENSION EXL WITH LM 06/25/2014
NIPRO DIAGNOSTICS, INC. TRUETRACK 06/05/2014
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION VISTA CLINICAL CHEMISTRY SYSTE 03/31/2014
NIPRO DIAGNOSTICS, INC. TRUETRACK 03/10/2014
NIPRO DIAGNOSTICS, INC. TRUETRACK 03/10/2014
NIPRO DIAGNOSTICS, INC. TRUETRACK 03/05/2014
NIPRO DIAGNOSTICS, INC. TRUERESULT 01/29/2014
SIEMENS HEALTHCARE DIAGNOSTICS INC DIMENSION VISTA 1500 01/10/2014
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