Agamatrix
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) | K241304 | WaveSense Jazz Blood Glucose Monitoring System | NBW | 2024-06-06 | View |
| 510(k) | K101597 | WAVESENSE DIABETES MANAGER MODEL VERSION 1.3.4 | NBW | 2010-10-18 | View |
| 510(k) | K073573 | WAVESENSE KEYNOTE CODELESS BLOOD GLUCOSE MONITORING SYSTEM | NBW | 2008-01-30 | View |
| 510(k) | K072413 | MODIFICATION TO: JAZZ BLOOD GLUCOSE MONITORING SYSTEM | NBW | 2007-09-27 | View |
| 510(k) | K071393 | JAZZ BLOOD GLUCOSE MONITORING SYSTEM | NBW | 2007-07-20 | View |
| 510(k) | K063409 | LIBERTY BLOOD GLUCOSE MONITORING SYSTEM, MODEL 8000-0067 | NBW | 2007-01-12 | View |
| 510(k) | K062434 | ZERO-CLICK DATA MANAGEMENT SYSTEM, MODEL 8000-01528 | NBW | 2006-11-13 | View |
No matching devices.
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