510(k) K213834 ยท DQX Wire, Guide, Catheter
Cardio Flow Peripheral Guide Wire
| Applicant | Cardio Flow Inc.,, Mahtomedi MN, US |
| Decision | Substantially Equivalent, Mar 18, 2022 |
| Received | Dec 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213834
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.