FDA 510(k) Applications Submitted by Reprobitech Corp.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172751 | 09/12/2017 | iVitri Straw | Reprobitech Corp. |
| K162640 | 09/22/2016 | iVitri EZ | REPROBITECH CORP. |
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