Mediaid, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K071642 | MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER | DQA | 2008-05-02 | View |
| 510(k) | K071610 | MEDIAID PULSE OXIMETER M30 AND M34 | DQA | 2007-11-05 | View |
| 510(k) | K061896 | MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101N | DQA | 2007-04-12 | View |
| 510(k) | K041964 | MEDIAID REUSABLE FINGER CLIP SPO2 SENSORS AND DISPOSABLE NON-ADHESIVE SENSORS AND ADHESIVE SPO2 SENSORS | DQA | 2004-09-14 | View |
No matching devices.
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