Hemosense, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K072727 | INRATIO 2 PT MONITORING SYSTEM | GJS | 2007-10-26 | View |
| 510(k) | K021923 | INRATIO SELF-TEST | GJS | 2002-10-24 | View |
| 510(k) | K020679 | INRATIO | GJS | 2002-05-06 | View |
No matching devices.
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