K240020
- 510(k) number
- K240020
- Device name
- Ziehm Vision FD
- Applicant
- Ziehm Imaging GmbH DE
- Product code
- OWB — Interventional Fluoroscopic X-Ray System
- Decision date
- 2024-01-30
- Date received
- 2024-01-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.2 MB · U.S. public domain
Also available from FDA: K240020.pdf
Official FDA record: K240020
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.