K233348
- 510(k) number
- K233348
- Device name
- 16 Breast Coil
- Applicant
- Philips Medical System Nederlands B.V. NL
- Product code
- MOS — Coil, Magnetic Resonance, Specialty
- Decision date
- 2023-10-24
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K233348.pdf
Official FDA record: K233348
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.