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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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13 records meeting your search criteria returned- Product Code: GXD Product Problem: Device Inoperable Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
NEUROTHERM, INC 3 LESION NT1100¿ PAIN MANAGEMENT RF GENE 08/17/2017
NEUROTHERM, INC 4 LESION NT2000¿ PAIN MANAGEMENT RF GENE 07/28/2017
COVIDIEN-PLYMOUTH GENERATOR WITH VERSION4.0.0 + 4.1.0 06/11/2015
STRYKER INSTRUMENTS-KALAMAZOO MULTIGEN RADIOFREQUENCY GENERATOR 04/06/2015
STRYKER INSTRUMENTS-KALAMAZOO RF GEN OBSOLETE REPLACED BY 0406900000 08/27/2014
NEUROTHERM INC NEUROTHERM RFA MACHINE 07/23/2014
NEUROTHERM INC NEUROTHERM RFA MACHINE 07/23/2014
NEUROTHERM NEUROTHERM 07/11/2014
STRYKER INSTRUMENTS-KALAMAZOO RF GEN OBSOLETE REPLACED BY 0406900000 06/27/2014
STRYKER INSTRUMENTS-KALAMAZOO MULTIGEN RADIOFREQUENCY GENERATOR 04/23/2014
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