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FDA 510(k) Applications for Medical Device Product Code "EAZ"
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| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K041614 | ADDENT, INC. | MICROLUX DL | 04/04/2005 |
| K072309 | ADDENT, INC. | MICROLUX/BLU | 11/19/2007 |
| K003995 | TRYLON CORP. | SPECULITE/ORALLITE | 03/16/2001 |
| K033033 | TRYLON CORP. | VIZILITE-BLUE ORAL EXAM KIT | 11/22/2004 |