FDA 510(k), K112844, REHASTIM 2, REHAMOVE 2
FDA 510(k), K112844, REHASTIM 2, REHAMOVE 2
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$149.00 USD
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510(K) Number: K112844
Device Name: REHASTIM 2, REHAMOVE 2
Manufacturer:
Device Classification Name: Stimulator, Neuromuscular, External Functional
Regulation Number: 882.5810
Classification Product Code: GZI
Date Received: 09/29/2011
Decision Date: 10/27/2011
Regulation Medical Specialty: Neurology
Device Name: REHASTIM 2, REHAMOVE 2
Manufacturer:
Device Classification Name: Stimulator, Neuromuscular, External Functional
Regulation Number: 882.5810
Classification Product Code: GZI
Date Received: 09/29/2011
Decision Date: 10/27/2011
Regulation Medical Specialty: Neurology