Device Classification Name |
stimulator, nerve, transcutaneous, over-the-counter
|
510(k) Number |
K131290 |
Device Name |
IQ TECHNOLOGIES |
Applicant |
IQ TECHNOLOGIES INC. |
1631 E. Sunset Road |
Suite C 103 |
Las Vegas,
NV
89119
|
|
Applicant Contact |
ELI JOSEF |
Correspondent |
IQ TECHNOLOGIES INC. |
1631 E. Sunset Road |
Suite C 103 |
Las Vegas,
NV
89119
|
|
Correspondent Contact |
ELI JOSEF |
Regulation Number | 882.5890
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 05/06/2013 |
Decision Date | 08/06/2014 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|