510(k) K191502 ยท DQX Wire, Guide, Catheter
Heraeus Peripheral Guidewire
| Applicant | Heraeus Medical Components, LLC, Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 26, 2019 |
| Received | Jun 6, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191502
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.