510(k) K233678 ยท IZL System, X-Ray, Mobile
Radiography 7000 M
| Applicant | Philips Medical Systems Dmc GmbH, Hamburg, DE |
| Decision | Substantially Equivalent, Feb 14, 2024 |
| Received | Nov 16, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233678
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 26, 2026 | Philips North America Model Number: 712010. Open, Classified |
IZL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.