Device Classification Name |
Device, Biofeedback
|
510(k) Number |
K900639 |
Device Name |
DYNATRON 350 EMG/BIOFEEDBACK ANALYZER |
Applicant |
DYNATRONICS LASER CORP. |
470 LAWNDALE DRIVE, BUILDING |
D |
SALT LAKE CITY,
UT
84115
|
|
Applicant Contact |
H CULLIMORE |
Correspondent |
DYNATRONICS LASER CORP. |
470 LAWNDALE DRIVE, BUILDING |
D |
SALT LAKE CITY,
UT
84115
|
|
Correspondent Contact |
H CULLIMORE |
Regulation Number | 882.5050
|
Classification Product Code |
|
Date Received | 02/09/1990 |
Decision Date | 10/04/1990 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|