510(k) K172090 ยท DQY Catheter, Percutaneous
GuideLiner V3 Catheter
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 20, 2017 |
| Received | Jul 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172090
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.