iVitri EZ — Reprobitech Corp. (510(k) K162640)
iVitri EZ — Reprobitech Corp. (510(k) K162640) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: iVitri EZ; Applicant: Reprobitech Corp.; Clearance track: 510(k).
| Device name | iVitri EZ |
|---|---|
| Applicant | Reprobitech Corp. |
| Clearance track | 510(k) |
| Submission number | K162640 |
| Decision | Substantially Equivalent |
| Decision date | 2017-06-30 |
| Date received | 2016-09-22 |
| Product code | MQK |
| Device class | 2 |
| Medical specialty | Obstetrics/Gynecology |
| Applicant location | NY, US |
| Source | openFDA device |
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$1999/mo
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