K222683 is an FDA 510(k) clearance for the Fibroid Mapping Reviewer Application (FMRA). This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).
Submitted by Nesa Medtech Private Limited (Bengaluru, IN). The FDA issued a Cleared decision on July 17, 2023, 314 days after receiving the submission on September 6, 2022.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.
| 510(k) Number | K222683 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 06, 2022 |
| Decision Date | July 17, 2023 |
| Days to Decision | 314 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | LLZ - System, Image Processing, Radiological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.2050 |