FDA 510(k) Applications for Medical Device Product Code "DEG"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K071712 | TECHLAB INC., CORPORATE RESEARCH CENTER | LEUKO EZ VUE | 12/04/2007 |
K011396 | TECHLAB, INC. | IBD-CHEK | 06/18/2001 |
K030704 | TECHLAB, INC. | IBD-QUIK CHEK | 04/21/2003 |
K042071 | TECHLAB, INC. | IBD-SCAN | 10/20/2004 |