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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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118 records meeting your search criteria returned- Product Code: LCP Product Problem: Incorrect Or Inadequate Test Results Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS COBAS 8000 C 502 MODULE 06/12/2017
TOSOH CORPORATION TOSOH HLC-723G8 ANALYZER G8 01/20/2017
TOSOH CORPORATION TOSOH HLC-723G8 ANALYZER G8 01/03/2017
TOSOH HI-TEC TOSOH G8 AUTOMATED HPLC ANALYZER 06/10/2016
SIEMENS HEALTHCARE DIAGNOSTICS DCA VANTAGE 10/01/2015
SIEMENS HEALTHCARE DIAGNOSTICS DCA ANALYZER 09/01/2015
SIEMENS HEALTHCARE DIAGNOSTICS DCA ANALYZER 09/01/2015
ROCHE DIAGNOSTICS TINA-QUANT HEMOGLOBIN A1C GEN.2 08/27/2015
SIEMENS HEALTHCARE DIAGNOSTICS DCA ANALYZER 08/25/2015
SIEMENS HEALTHCARE DIAGNOSTICS DCA VANTAGE 04/08/2015
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