K240796
- 510(k) number
- K240796
- Device name
- myAblation Guide (VB80A)
- Applicant
- Siemens Healthcare GmbH DE
- Product code
- QTZ — Radiological Image Processing Software For Ablation
- Decision date
- 2024-08-06
- Date received
- 2024-03-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K240796.pdf
Official FDA record: K240796
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.