Amplife Corporation
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) | K050413 | AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600 | DXN | 2005-03-04 | View |
| 510(k) | K043550 | AMPLIFE UPPER ARM BLOOD PRESSURE MONITOR, MODEL M100 | DXN | 2005-01-27 | View |
| 510(k) | K042906 | AMPLIFE DIGITAL INFRARED EAR THERMOMETER, MODEL E101 | FLL | 2004-11-19 | View |
| 510(k) | K042575 | AMPLIFE DIGITAL CLINICAL THERMOMETER | FLL | 2004-09-30 | View |
No matching devices.
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