K233930
- 510(k) number
- K233930
- Device name
- MRCP+ version 2 (MRCP+ v2)
- Applicant
- Perspectum GB
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2024-03-13
- Date received
- 2023-12-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K233930.pdf
Official FDA record: K233930
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.