FDA 510(k) Applications for Medical Device Product Code "LJB"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K974552 | DIAMEDIX CORP. | DIAMEDIX IS-MEASLES IGG TEST SYSTEM | 01/28/1998 |
K971620 | INOVA DIAGNOSTICS, INC. | QUANTA LITE RUBEOLA (MEASLES) IGG | 07/22/1997 |