K233444
- 510(k) number
- K233444
- Device name
- InkSpace Imaging Small Body Array
- Applicant
- Inkspace Imaging, Inc. CA · US
- Product code
- MOS — Coil, Magnetic Resonance, Specialty
- Decision date
- 2024-01-08
- Date received
- 2023-10-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K233444.pdf
Official FDA record: K233444
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.