Device Classification Name |
Device, Biofeedback
|
510(k) Number |
K914920 |
Device Name |
BIOFEEDBACK SYSTEM/3 |
Applicant |
DAVICON, INC. |
C/O MEDICAL DEVICE CONSULTANTS |
45 WEST STREET, SUITE 2 |
ATTLEBORO,
MA
02703
|
|
Applicant Contact |
LYNNE ARONSON |
Correspondent |
DAVICON, INC. |
C/O MEDICAL DEVICE CONSULTANTS |
45 WEST STREET, SUITE 2 |
ATTLEBORO,
MA
02703
|
|
Correspondent Contact |
LYNNE ARONSON |
Regulation Number | 882.5050
|
Classification Product Code |
|
Date Received | 11/04/1991 |
Decision Date | 11/16/1992 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|