K262294
- 510(k) number
- K262294
- Device name
- dS FootAnkle 16Ch 1.5T;dS FootAnkle 16Ch 3.0T;dS HiRes Hand/Wrist 16Ch 1.5T;dS HiRes Hand/Wrist 16CH 3.0T;dS Small Extremity 16Ch 1.5T;dS Small Extremity 16Ch 3.0T
- Applicant
- Philips Medical Systems Nederland B.V. NL
- Product code
- MOS — Coil, Magnetic Resonance, Specialty
- Decision date
- 2026-07-24
- Date received
- 2026-07-07
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K262294.pdf
Official FDA record: K262294
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.