Device Classification Name |
fluorometer, for clinical use
|
510(k) Number |
K962919 |
Device Name |
VITROS IMMUNODIAGNOSTIC SYSTEM |
Applicant |
JOHNSON & JOHNSON CLINICAL DIAGNOSTICS, INC. |
100 INDIGO CREEK DR. |
ROCHESTER,
NY
14650 -0882
|
|
Applicant Contact |
CHARLES C MORGANSON, JR. |
Correspondent |
JOHNSON & JOHNSON CLINICAL DIAGNOSTICS, INC. |
100 INDIGO CREEK DR. |
ROCHESTER,
NY
14650 -0882
|
|
Correspondent Contact |
CHARLES C MORGANSON, JR. |
Regulation Number | 862.2560
|
Classification Product Code |
|
Date Received | 07/26/1996 |
Decision Date | 10/18/1996 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Clinical Chemistry
|
510k Review Panel |
Clinical Chemistry
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|