Diagnostic Devices, 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) | K090307 | DDI ULTRASONIC NEBULIZER SYSTEM | CAF | 2009-06-18 | View |
| 510(k) | K073118 | PRODIGY VOICE BLOOD GLUCOSE MONITORING SYSTEM | NBW | 2008-03-05 | View |
| 510(k) | K060467 | PRODIGY BLOOD GLUCOSE TEST SYSTEM | NBW | 2006-07-13 | View |
| 510(k) | K053593 | PRODIGY | NBW | 2006-07-06 | View |
No matching devices.
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