K243033
- 510(k) number
- K243033
- Device name
- dS Wrist coil 8ch 1.5T
- Applicant
- Philips Medical Systems Nederland B.V. NL
- Product code
- MOS — Coil, Magnetic Resonance, Specialty
- Decision date
- 2024-10-18
- Date received
- 2024-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K243033.pdf
Official FDA record: K243033
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.