FDA 510(k) Applications Submitted by CRUXELL Corp.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K211317 | 04/30/2021 | CRUXVIEW | CRUXELL Corp. |
| K183637 | 12/26/2018 | Cruxcan (CRX-1000) | Cruxell Corp. |
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