Device Classification Name |
Stimulator, Nerve, Transcutaneous, For Pain Relief
More FDA Info for this Device |
510(K) Number |
K032653 |
Device Name |
Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant |
MICRO CURRENT TECHNOLOGY, INC.
4822 CALIFORNIA AVE., S.W.,
SUITE 201
SEATTLE, WA 98116 US
Other 510(k) Applications for this Company
|
Contact |
DAVID SUZUKI
Other 510(k) Applications for this Contact |
Regulation Number |
882.5890
More FDA Info for this Regulation Number |
Classification Product Code |
GZJ
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
08/28/2003 |
Decision Date |
09/12/2003 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
NE - Neurology |
Review Advisory Committee |
NE - Neurology |
Statement / Summary / Purged Status |
Statement |
Type |
Traditional |
Reviewed By Third Party |
Y |
Expedited Review |
|