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

 
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202 records meeting your search criteria returned- Product Code: LKK Product Problem: Failure to Interrogate Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 12/30/2015
MEDTRONIC NEUROMODULATION N'VISION 12/18/2015
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 11/30/2015
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 11/03/2015
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 11/02/2015
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/26/2015
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 10/26/2015
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 10/13/2015
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 09/18/2015
MEDTRONIC NEUROMODULATION SYNCHROMED II 09/09/2015
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