SOLUTIS — Quantel Medical (510(k) K130933)
SOLUTIS — Quantel Medical (510(k) K130933) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: SOLUTIS; Applicant: Quantel Medical; Clearance track: 510(k).
| Device name | SOLUTIS |
|---|---|
| Applicant | Quantel Medical |
| Clearance track | 510(k) |
| Submission number | K130933 |
| Decision | Substantially Equivalent |
| Decision date | 2013-08-02 |
| Date received | 2013-04-04 |
| Product code | HQF |
| Device class | 2 |
| Medical specialty | Ophthalmic |
| Applicant location | MA, US |
| Source | openFDA device |
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