K240822
- 510(k) number
- K240822
- Device name
- Image Management V15
- Applicant
- Philips Medical Systems Technologies IL
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-04-24
- Date received
- 2024-03-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K240822.pdf
Official FDA record: K240822
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.