510(k) K201081 ยท DQK Computer, Diagnostic, Programmable
AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter
| Applicant | Philips Medical System Nederland B.V., Best, NL |
| Decision | Substantially Equivalent, Dec 17, 2020 |
| Received | Apr 22, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201081
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.