510(k) K201690 ยท DQX Wire, Guide, Catheter
Mirage Hydrophilic Guidewire; X-pedion Hydrophilic Guidewire
| Applicant | Micro Therapeutics, Inc. d/b/a ev3 Neurovascular, Irvine CA, US |
| Decision | Substantially Equivalent, Jul 21, 2020 |
| Received | Jun 22, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K201690
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.