K241751
- 510(k) number
- K241751
- Device name
- NeuroLF (Basic); NeuroLF (Pro); NeuroLF (Advanced); NeuroLF Seat
- Applicant
- Positrigo AG CH
- Product code
- KPS — System, Tomography, Computed, Emission
- Decision date
- 2024-07-15
- Date received
- 2024-06-18
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Flag
- Third-party review
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.8 MB · U.S. public domain
Also available from FDA: K241751.pdf
Official FDA record: K241751
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.