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FDA 510(k) Applications for Medical Device Product Code "FJD"
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| 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 |