Resmed Germany, 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) | K131932 | APNEALINK PRO | MNR | 2013-11-08 | View |
| 510(k) | K122715 | STELLAR 150 | MNT | 2013-06-17 | View |
| 510(k) | K113640 | STELLAR 150 | MNT | 2012-04-05 | View |
| 510(k) | K103167 | STELLAR 150 | MNT | 2011-03-01 | View |
| 510(k) | K083575 | APNEALINK PLUS, MODEL: 22328 | MNR | 2009-03-19 | View |
| 510(k) | K070263 | APNEALINK | MNR | 2007-06-15 | View |
| 510(k) | K061405 | APNEALINK, MODEL 22302 | MNR | 2006-07-25 | View |
No matching devices.
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