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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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95 records meeting your search criteria returned- Product Code: CFR Report Date From: 1/1/2017 Report Date To: 12/31/2017

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ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS GLUC3 GLUCOSE HK GEN.3 10/23/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION VISTA 1500 10/20/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA 2400 10/13/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA 2400 10/13/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA 2400 10/13/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION VISTA 1500 10/12/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION VISTA 1500 10/12/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION VISTA 1500 10/11/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA 1800 10/11/2017
ROCHE DIAGNOSTICS COBAS 8000 C 702 MODULE 10/11/2017
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