Device Classification Name |
Arthrometer
|
510(k) Number |
K812806 |
Device Name |
KT-1000 DEVICE |
Applicant |
|
Correspondent |
|
Regulation Number | 890.1615
|
Classification Product Code |
|
Date Received | 10/06/1981 |
Decision Date | 11/10/1981 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Physical Medicine
|
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|