510(k) K223918 ยท DQK Computer, Diagnostic, Programmable
AltaTrack Equipment R1.2, AltaTrack Guidewire, AltaTrack 3D Hub
| Applicant | Philips Medical Systems Nederland B.V., Best, NL |
| Decision | Substantially Equivalent, Jun 8, 2023 |
| Received | Dec 29, 2022 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K223918
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.