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FDA 510(k) Applications for Medical Device Product Code "CFQ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K990551 | DADE BEHRING, INC. | IGG FLEX REAGENT CARTRIDGE | 03/25/1999 |
K990553 | DADE BEHRING, INC. | IGM FLEX REAGENT CARTRIDGE | 03/22/1999 |
K990552 | DADE BEHRING, INC. | IMMUNOGLOBULIN A TEST SYSTEM | 03/25/1999 |
K981786 | THE BINDING SITE, LTD. | IGA MININEPH ANTISERUM | 11/24/1999 |