iQFlex Pro — First Source, Inc. (510(k) K240009)
iQFlex Pro — First Source, Inc. (510(k) K240009) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: iQFlex Pro; Applicant: First Source, Inc.; Clearance track: 510(k).
| Device name | iQFlex Pro |
|---|---|
| Applicant | First Source, Inc. |
| Clearance track | 510(k) |
| Submission number | K240009 |
| Decision | Substantially Equivalent |
| Decision date | 2024-07-03 |
| Date received | 2024-01-02 |
| Product code | IZL |
| Device class | 2 |
| Medical specialty | Radiology |
| Applicant location | NY, US |
| Source | openFDA device |
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