K232910
- 510(k) number
- K232910
- Device name
- CombiDiagnost R90
- Applicant
- Philips Medical Systems Dmc GmbH DE
- Product code
- JAA — System, X-Ray, Fluoroscopic, Image-Intensified
- Decision date
- 2023-10-19
- Date received
- 2023-09-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232910.pdf
Official FDA record: K232910
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.