FDA 510(k) Applications Submitted by DIAGNOSTIC DEVICES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060467 | 02/23/2006 | PRODIGY BLOOD GLUCOSE TEST SYSTEM | DIAGNOSTIC DEVICES, INC. |
| K090307 | 02/06/2009 | DDI ULTRASONIC NEBULIZER SYSTEM | DIAGNOSTIC DEVICES, INC. |
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