K240157
- 510(k) number
- K240157
- Device name
- InVision 1.5 Surgical Theatre
- Applicant
- Deerfield Imaging, Inc. MN · US
- Product code
- LNH — System, Nuclear Magnetic Resonance Imaging
- Decision date
- 2024-02-15
- Date received
- 2024-01-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K240157.pdf
Official FDA record: K240157
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.