Caradyne, Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
Advertisement
Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K040862 | GUARDIAN NEONATE CPAP/HUMIDIFICATION SYSTEM | BZD | 2004-06-30 | View |
| 510(k) | K023565 | OXICHECK | CCL | 2003-03-28 | View |
| 510(k) | K000959 | CRITERION 60 OR PM 60 | CAP | 2000-06-22 | View |
| 510(k) | K992101 | CRITERION 40 OR PM 40 | CAP | 2000-01-06 | View |
| 510(k) | K982283 | WHISPERFLOW OXYGEN FLOW GENERATOR - ADJUSTABLE MODEL WF 8500 WHISPERFLOW OXYGEN FLOW GENERATOR - FIXED MODEL WF 8530 WH | BYE | 1999-03-09 | View |
No matching devices.
Advertisement