PRODIGY BLOOD GLUCOSE TEST SYSTEM — Diagnostic Devices, Inc. (510(k) K060467)
PRODIGY BLOOD GLUCOSE TEST SYSTEM — Diagnostic Devices, Inc. (510(k) K060467) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PRODIGY BLOOD GLUCOSE TEST SYSTEM; Applicant: Diagnostic Devices, Inc.; Clearance track: 510(k).
| Device name | PRODIGY BLOOD GLUCOSE TEST SYSTEM |
|---|---|
| Applicant | Diagnostic Devices, Inc. |
| Clearance track | 510(k) |
| Submission number | K060467 |
| Decision | Substantially Equivalent |
| Decision date | 2006-07-13 |
| Date received | 2006-02-23 |
| Product code | NBW |
| Device class | 2 |
| Medical specialty | Clinical Chemistry |
| Applicant location | IL, US |
| Source | openFDA device |
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