FDA 510(k) Applications for Medical Device Product Code "LNX"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K102135 | NUVON, INC. | VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM | 10/22/2010 |
K043529 | ROCHE DIAGNOSTICS CORP. | ACCU-CHEK ADVISOR INSULIN GUIDANCE SOFTWARE | 04/08/2005 |
K100066 | WELLDOC, INC | DIABETESMANAGER SYSTEM, DIABETESMANAGER-RX SYSTEM MODEL VERSION 1.1 | 07/15/2010 |