Device Classification Name |
Device, Biofeedback
|
510(k) Number |
K925750 |
Device Name |
RELAXOMAT |
Applicant |
RELAXOMAT, INC. |
C/O GUITO & ASSOCIATES |
4214 EL PRADO BLVD. |
TAMPA,
FL
33629
|
|
Applicant Contact |
RALPH M GUITO |
Correspondent |
RELAXOMAT, INC. |
C/O GUITO & ASSOCIATES |
4214 EL PRADO BLVD. |
TAMPA,
FL
33629
|
|
Correspondent Contact |
RALPH M GUITO |
Regulation Number | 882.5050
|
Classification Product Code |
|
Date Received | 11/13/1992 |
Decision Date | 01/31/1995 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|