FDA 510(k) Applications for Medical Device Product Code "EJB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K140144 | CENTRIX, INC. | BENDA WEDGE | 07/08/2014 |
K981234 | LONE STAR TECHNOLOGIES | FLARE,FILE, FILL | 06/05/1998 |
K023367 | NEKS TECHNOLOGIES | DETECTAR, MODEL N123-MI | 06/25/2003 |