FDA 510(k) Applications Submitted by Rolence Enterprise Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K202369 | 08/19/2020 | RXS 1000 | Rolence Enterprise Inc. |
| K172928 | 09/25/2017 | Portable X-ray System | Rolence Enterprise Inc. |
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