510(k) K200120 ยท DQX Wire, Guide, Catheter
LiteSaber Wire Torque Assist Device
| Applicant | Vesatek, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, May 7, 2020 |
| Received | Jan 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200120
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.