K243473 is an FDA 510(k) clearance for the PRORAD ATLAS ULTRAPORTABLE. This device is classified as a System, X-ray, Mobile (Class II - Special Controls, product code IZL).
Submitted by Prognosys Medical Systems Private Limited (Bengaluru, IN). The FDA issued a Cleared decision on July 29, 2025, 263 days after receiving the submission on November 8, 2024.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1720.
| 510(k) Number | K243473 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 08, 2024 |
| Decision Date | July 29, 2025 |
| Days to Decision | 263 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 |