DV. Target
FDA 510(k) K202928 · Deepvoxel, Inc.
510(k) numberK202928
Submission
- Device name
- DV. Target
- Applicant
- Deepvoxel, Inc.
Irvine, CA, US - Received
- September 29, 2020
- Decision date
- April 2, 2021
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QKB – Radiological Image Processing Software For Radiation Therapy
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.2050
- Specialty
- Radiology
To provide semi-automatic or fully-automated radiological image processing and analysis tools for radiation therapy. Software implementing artificial intelligence (AI) including nonadaptive machine learning algorithms trained with clinical and/or artificial radiological images. In these devices, the algorithm training images typically impact device performance. AI based radiological image…
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|---|---|---|---|
| K262452 | AutoContour (RADAC V6)QKB · Special | Radformation, Inc. | 08/14/2026SE |
| K261306 | AI Contouring (VA10A)QKB · Traditional | Varian Medical Systems | 07/10/2026SE |
| K260528 | OncoStudioQKB · Traditional | Oncosoft. Inc., | 07/02/2026SE |
| K252548 | AI-Rad Companion Organs RTQKB · Traditional | Siemens Healthcare GmbH | 04/10/2026SE |
| K252190 | DeepBT Detector-PlusQKB · Traditional | Aitewan Biomedical Technology, Inc. | 04/10/2026SE |
| K253270 | Contour ProtégéAI+QKB · Traditional | Mim Software, Inc. | 03/27/2026SE |
| K260509 | AutoContour (RADAC V5)QKB · Special | Radformation, Inc. | 03/19/2026SE |
| K251306 | Seg Pro V3 (RT-300)QKB · Traditional | Ever Fortune.Ai, Co., Ltd. | 01/28/2026SE |
| K251351 | AccuContour 4.0QKB · Traditional | Manteia Technologies Co., Ltd. | 01/23/2026SE |
| K250780 | ARTAssistantQKB · Traditional | Manteia Technologies Co., Ltd. | 12/05/2025SE |
Questions and answers
When was DV. Target cleared by the FDA?
DV. Target (K202928) received a 510(k) decision of Substantially Equivalent on April 2, 2021, 185 days after the submission was received.
What is the product code of K202928?
The FDA product code is QKB – Radiological Image Processing Software For Radiation Therapy, a Class II (moderate risk) device regulated under 21 CFR 892.2050.