K233600
- 510(k) number
- K233600
- Device name
- Smart Fit Knee 3.0T
- Applicant
- Philips Healthcare (Suzhou) Co., Ltd. CN
- Product code
- MOS — Coil, Magnetic Resonance, Specialty
- Decision date
- 2024-02-05
- Date received
- 2023-11-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K233600.pdf
Official FDA record: K233600
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.