510(k) K232910 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
CombiDiagnost R90
| Applicant | Philips Medical Systems Dmc GmbH, Hamburg, DE |
| Decision | Substantially Equivalent, Oct 19, 2023 |
| Received | Sep 19, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232910
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 7, 2025 | Philips Medical Systems DMC GmbH CombiDiagnost R90;
Model Number: 709031; Open, Classified |
JAA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.