Lxn Corp.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K002688 | PERSONAL GLUCOSE CONTROL CHARTING SYSTEM | CGA | 2001-02-01 | View |
| 510(k) | K991754 | GO GLUCOSE MONITORING SYSTEM | CGA | 1999-09-08 | View |
| 510(k) | K990942 | DUET II GLUCOSE CONTROL MONITORING SYSTEM | CGA | 1999-08-02 | View |
| 510(k) | K973140 | DUET GLUCOSE CONTROL MONITORING SYSTEM | CGA | 1997-10-31 | View |
| 510(k) | K962597 | LXN FRUCTOSAMINE TEST SYSTEM | LCP | 1997-06-13 | View |
| 510(k) | K960034 | LXN BLOOD GLUCOSE TEST SYSTEM | CGA | 1996-06-28 | View |
| 510(k) | K955629 | LXN FRUCTOSAMINE TEST | JJX | 1996-03-20 | View |
No matching devices.
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