K233652
- 510(k) number
- K233652
- Device name
- Contour Hand/Wrist (Q7000232)
- Applicant
- Quality Electrodynamics OH · US
- Product code
- MOS — Coil, Magnetic Resonance, Specialty
- Decision date
- 2024-02-16
- Date received
- 2023-11-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233652.pdf
Official FDA record: K233652
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.