Device Classification Name |
Device, Biofeedback
|
510(k) Number |
K892114 |
Device Name |
ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM |
Applicant |
ECLOSION, INC. |
3960-A NIAGARA ST. |
DENVER,
CO
80207
|
|
Applicant Contact |
FRANK DIMAURO |
Correspondent |
ECLOSION, INC. |
3960-A NIAGARA ST. |
DENVER,
CO
80207
|
|
Correspondent Contact |
FRANK DIMAURO |
Regulation Number | 882.5050
|
Classification Product Code |
|
Date Received | 03/30/1989 |
Decision Date | 10/13/1989 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|