510(k) K201834 ยท DQX Wire, Guide, Catheter
HI-TORQUE PROCEED Guide Wire Family
| Applicant | Abbott Vascular, Santa Clara CA, US |
| Decision | Substantially Equivalent, Jul 30, 2020 |
| Received | Jul 2, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K201834
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.