K250181
- 510(k) number
- K250181
- Device name
- AV Viewer
- Applicant
- Philips Medical Systems Nederland B.V. NL
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2025-07-15
- Date received
- 2025-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K250181.pdf
Official FDA record: K250181
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.