K221417 is an FDA 510(k) clearance for the CLAROX plus (Model: VX-100). This device is classified as a System, X-ray, Mobile (Class II - Special Controls, product code IZL).
Submitted by Vsi Co., Ltd. (Cheongju-Si, KR). The FDA issued a Cleared decision on September 13, 2022, 120 days after receiving the submission on May 16, 2022.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1720.
| 510(k) Number | K221417 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 16, 2022 |
| Decision Date | September 13, 2022 |
| Days to Decision | 120 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | IZL - System, X-ray, Mobile |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1720 |