NEUROTECH RECOVERY


Device Classification Name

electrode, cutaneous

510(k) Number K112934
Device Name NEUROTECH RECOVERY
Applicant
BIO-MEDICAL RESEARCH, LTD.
bmr house
parkmore business park, west
galway, 

IE

el

Applicant Contact anne-marie keenan
Correspondent
BIO-MEDICAL RESEARCH, LTD.
bmr house
parkmore business park, west
galway, 

IE

el

Correspodent Contact anne-marie keenan
Regulation Number 882.1320
Classification Product Code
GXY  
Date Received 10/03/2011
Decision Date 01/20/2012
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No