O-Two Medical Technologies, Inc.
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) | K173205 | Equinox Advantage | BZR | 2018-08-29 | View |
| 510(k) | K113687 | EQUINOX RELIEVE | BZR | 2012-04-30 | View |
| 510(k) | K112546 | O_TWO CPAP SYSTEM | BYE | 2011-12-27 | View |
| 510(k) | K093862 | CAREVENT HANDHELD CPAP SYSTEM | BTL | 2010-05-06 | View |
| 510(k) | K081330 | CAREVENT PAR (PUBLIC ACCESS RESUSCITATOR) | BTL | 2009-03-06 | View |
| 510(k) | K051469 | CAREVENT ATV+ AND CAREVENT MRI | BTL | 2005-09-28 | View |
| 510(k) | K051889 | CAREVENT CA AND DRA | BTL | 2005-08-30 | View |
No matching devices.
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