Cleveland Medical Devices, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K063872 | KINESIA | GYD | 2007-04-06 | View |
| 510(k) | K042039 | FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120 | OLV | 2004-11-17 | View |
| 510(k) | K013863 | CRYSTAL MONITOR MODEL 16 | OMC | 2002-02-19 | View |
| 510(k) | K001110 | CRYSTAL-EEG MODEL 15 | OMC | 2000-07-05 | View |
| 510(k) | K970672 | CRYSTAL-EEG MODEL 10 (MODEL 10) | OMC | 1997-05-22 | View |
| 510(k) | K964690 | LIBERTY VALVE | KNX | 1997-03-21 | View |
| 510(k) | K962591 | FOOT WEIGHT ALARM | IRN | 1996-12-04 | View |
| 510(k) | K954670 | PRESSORE MONITOR | IKE | 1995-10-30 | View |
No matching devices.
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