Device Classification Name |
Radioimmunoassay, Luteinizing Hormone
|
510(k) Number |
K874032 |
Device Name |
IRMA-COUNT LH W/MONO. ANTIBODIES RKLH1,2,5 |
Applicant |
DIAGNOSTIC PRODUCTS CORP. |
5700 WEST 96TH ST. |
LOS ANGELES,
CA
90045 -5597
|
|
Applicant Contact |
B ASARCH,PHD |
Correspondent |
DIAGNOSTIC PRODUCTS CORP. |
5700 WEST 96TH ST. |
LOS ANGELES,
CA
90045 -5597
|
|
Correspondent Contact |
B ASARCH,PHD |
Regulation Number | 862.1485
|
Classification Product Code |
|
Date Received | 10/02/1987 |
Decision Date | 12/30/1987 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Clinical Chemistry
|
510k Review Panel |
Clinical Chemistry
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|