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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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103 records meeting your search criteria returned- Product Code: IYE Patient Problem: No Patient Involvement Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ELEKTA LTD IVIEWGT 11/24/2015
CHRISTOPHER IVICEVICH - DIRECTOR OF RA/Q MOSAIQ 11/20/2015
ELEKTA INC MOSAIQ 11/11/2015
CHRISTOPHER IVICEVICH - DIRECTOR OF RA/Q MOSAIQ 11/04/2015
CHRISTOPHER IVICEVICH - DIRECTOR OF RA/Q MOSAIQ 11/04/2015
CHRISTOPHER IVICEVICH - DIRECTOR OF RA/Q MOSAIQ 11/04/2015
CHRISTOPHER IVICEVICH - DIRECTOR OF RA/Q MOSAIQ 10/29/2015
CHRISTOPHER IVICEVICH - DIRECTOR OF RA/Q MOSAIQ 09/23/2015
SIEMENS HEALTHCARE GMBH SYNGO RT THERAPIST 09/22/2015
CHRISTOPHER IVICEVICH - DIRECTOR OF RA/Q MOSAIQ 08/22/2015
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