FDA 510(k) Applications for Medical Device Product Code "FJD"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K042322 | HACH COMPANY | STERICHEK BLOOD LEAK REAGENT STRIPS | 12/07/2004 |
K123805 | REPROCESSING PRODUCTS CORP. | E-Z CHEK BLOOD LEAK TEST STRIPS | 03/20/2013 |
K990206 | SERIM RESEARCH CORP. | SERIM BLOOD LEAK TEST STRIP | 04/21/1999 |
K012115 | SERIM RESEARCH CORP. | SERIM BLOOD LEAK TEST STRIP-2 | 11/30/2001 |