510(k) K252645 ยท DQK Computer, Diagnostic, Programmable
LumiGuide Equipment R2.1; LumiGuide Wire; LumiGuide 3D Hub
| Applicant | Philips Medical Systems Nederland B.V., Best, NL |
| Decision | Substantially Equivalent, Oct 24, 2025 |
| Received | Aug 21, 2025 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K252645
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.