K954198 is the FDA 510(k) clearance record for VOXCAM, a class II device, cleared for Voxel on under FDA product code LMC (Camera, Multi Format, Radiological). FDA records list 3 510(k) clearances for Voxel. As of , FDA records show no recalls naming K954198.
Clearance record
Clearances, product code LMC
Trailing 12 monthsFDA records hold no clearances under product code LMC in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
