510(k) K233853 ยท DQK Computer, Diagnostic, Programmable
LumiGuide Wire; LumiGuide Equipment R2.0; LumiGuide 3D Hub
| Applicant | Philips Medical Systems Nederland B.V., Best, NL |
| Decision | Substantially Equivalent, Mar 14, 2024 |
| Received | Dec 5, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233853
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.