FDA 510(k) Applications for Medical Device Product Code "LFP"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K992847 | ELAN HOLDINGS, INC. | HICHEM BUN REAGENT | 10/14/1999 |
K990039 | GAMBRO HEALTHCARE | GAMBRO DQM 200 | 01/27/2000 |
K963537 | SIGMA DIAGNOSTICS, INC. | SIGMA DIAGNOSTICS BUN REAGENT | 10/24/1996 |