K253264
- 510(k) number
- K253264
- Device name
- myAblation Guide (VC10A)
- Applicant
- Siemens Healthcare GmbH DE
- Product code
- QTZ — Radiological Image Processing Software For Ablation
- Decision date
- 2026-06-16
- Date received
- 2025-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K253264.pdf
Official FDA record: K253264
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.