Device Classification Name |
Goniometer, Ac-Powered
|
510(k) Number |
K812908 |
Device Name |
ELECTRO-GONIOMETER |
Applicant |
CHATTANOOGA GROUP, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Correspondent |
CHATTANOOGA GROUP, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Regulation Number | 888.1500
|
Classification Product Code |
|
Date Received | 10/19/1981 |
Decision Date | 11/24/1981 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|