Voxel Dosimetry (00859873006226)
FDA 510(k) K243919 · Hermes Medical Solutions AB
510(k) numberK243919
Submission
- Device name
- Voxel Dosimetry (00859873006226)
- Applicant
- Hermes Medical Solutions AB
Stockholm, SE - Received
- December 20, 2024
- Decision date
- July 30, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QIH – Automated Radiological Image Processing Software
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.2050
- Specialty
- Radiology
To provide automated radiological image processing and analysis tools. Software implementing artificial intelligence including nonadaptive machine learning algorithms trained with clinical and/or artificial data. In these devices, the algorithm training data typically impacts device performance. Adaptive AI algorithms are not within scope of this product code.
Other 510(k)s with product code QIH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261795 | Quicktome Software SuiteQIH · Traditional | Omniscient Neurotechnology Pty, Ltd. | 09/10/2026SE |
| K260879 | 4DMQIH · Traditional | Invia, LLC | 09/10/2026SE |
| K251417 | ReVISION 2QIH · Traditional | Argus Cognitive, Inc. | 09/09/2026SE |
| K260525 | NextMR SpineQIH · Traditional | MRI2CT, Inc. | 09/04/2026SE |
| K260811 | Heartvue.ProtonQIH · Traditional | Heartvue.ai, Inc. | 08/26/2026SE |
| K261595 | Ceevra Reveal 4QIH · Traditional | Ceevra, Inc. | 08/25/2026SE |
| K262127 | DS Core CBCT AnatomyQIH · Traditional | Dentsply Sirona | 08/21/2026SE |
| K260584 | BoneMRIQIH · Traditional | Mriguidance B.V. | 08/21/2026SE |
| K261641 | Lower Limb AI (LLAI)QIH · Traditional | AI Planning Logic, Inc. | 08/18/2026SE |
| K253794 | Prostate CoreQIH · Traditional | Lucida Medical, Ltd. | 08/10/2026SE |
More from Lucida Medical, Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K253835 | AffinityQIH · Traditional | 07/31/2026SE |
| K252477 | Hybrid Viewer (00859873006240)KPS · Special | 09/09/2025SE |
| K241364 | Hybrid Viewer (00859873006189)KPS · Traditional | 11/08/2024SE |
| K202882 | AffinityKPS · Traditional | 12/23/2020SE |
| K193152 | AffinityKPS · Traditional | 02/14/2020SE |
| K191216 | Voxel Dosimetry v1.0LLZ · Traditional | 10/17/2019SE |
| K181468 | Hybrid3DKPS · Traditional | 10/25/2018SE |
| K171719 | Hybrid3DKPS · Traditional | 11/21/2017SE |
| K171681 | Hermes Medical Imaging Suite v5.7KPS · Traditional | 11/21/2017SE |
| K163687 | Olinda ExmIYX · Traditional | 07/19/2017SE |
Questions and answers
When was Voxel Dosimetry (00859873006226) cleared by the FDA?
Voxel Dosimetry (00859873006226) (K243919) received a 510(k) decision of Substantially Equivalent on July 30, 2025, 222 days after the submission was received.
What is the product code of K243919?
The FDA product code is QIH – Automated Radiological Image Processing Software, a Class II (moderate risk) device regulated under 21 CFR 892.2050.