Device Classification Name |
Device, Biofeedback
|
510(k) Number |
K852963 |
Device Name |
MYO-ACTUATOR |
Applicant |
VERIMED HOLDINGS, INC. |
2888 NE 25TH. COURT |
FORT LAUDERDALE,
FL
33305
|
|
Applicant Contact |
WILLIAM W MEE |
Correspondent |
VERIMED HOLDINGS, INC. |
2888 NE 25TH. COURT |
FORT LAUDERDALE,
FL
33305
|
|
Correspondent Contact |
WILLIAM W MEE |
Regulation Number | 882.5050
|
Classification Product Code |
|
Date Received | 07/12/1985 |
Decision Date | 01/21/1986 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|