K233678
- 510(k) number
- K233678
- Device name
- Radiography 7000 M
- Applicant
- Philips Medical Systems Dmc GmbH DE
- Product code
- IZL — System, X-Ray, Mobile
- Decision date
- 2024-02-14
- Date received
- 2023-11-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233678.pdf
Official FDA record: K233678
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.