Device Classification Name |
Recorder, Attention Task Performance
|
510(k) Number |
K854903 |
FOIA Releasable 510(k) |
K854903
|
Device Name |
GORDON DIAGNOSTIC SYSTEM MODEL I |
Applicant |
CLINICAL DIAGNOSTICS, INC. |
300 E. MINERAL AVE., #6 |
LITTLETON,
CO
80122
|
|
Applicant Contact |
BRUCE MEYER |
Correspondent |
CLINICAL DIAGNOSTICS, INC. |
300 E. MINERAL AVE., #6 |
LITTLETON,
CO
80122
|
|
Correspondent Contact |
BRUCE MEYER |
Classification Product Code |
|
Date Received | 12/09/1985 |
Decision Date | 06/02/1986 |
Decision |
Substantially Equivalent
(SESE) |
510k Review Panel |
Neurology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|