Device Classification Name |
stimulator, nerve, battery-powered
|
510(k) Number |
K823583 |
Device Name |
MYOTEST NERVE STIMULATOR |
Applicant |
PROTHIA USA, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Correspondent |
PROTHIA USA, INC. |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Regulation Number | 868.2775
|
Classification Product Code |
|
Date Received | 12/06/1982 |
Decision Date | 12/30/1982 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|