510(k) K191687 ยท DQX Wire, Guide, Catheter
pORTAL Steerable Hydrophilic Guidewire and pORTAL EXT Extension Wire
| Applicant | Phenox Limited, Galway, IE |
| Decision | Substantially Equivalent, Oct 9, 2019 |
| Received | Jun 24, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191687
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.