FDA 510(k), K093138, MT9000 SERIES ELECTRO-STIMULATOR, MODELS MT9000, MT9002, MT9001, MT9004 AND MT9003
FDA 510(k), K093138, MT9000 SERIES ELECTRO-STIMULATOR, MODELS MT9000, MT9002, MT9001, MT9004 AND MT9003
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510(K) Number: K093138
Device Name: MT9000 SERIES ELECTRO-STIMULATOR, MODELS MT9000, MT9002, MT9001, MT9004 AND MT9003
Manufacturer: SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD.
Device Classification Name: stimulator, muscle, powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 10/05/2009
Decision Date: 02/12/2010
Regulation Medical Specialty: Physical Medicine
Device Name: MT9000 SERIES ELECTRO-STIMULATOR, MODELS MT9000, MT9002, MT9001, MT9004 AND MT9003
Manufacturer: SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD.
Device Classification Name: stimulator, muscle, powered
Regulation Number: 890.5850
Classification Product Code: IPF
Date Received: 10/05/2009
Decision Date: 02/12/2010
Regulation Medical Specialty: Physical Medicine