510(k) K091750 ยท DQY Catheter, Percutaneous
GUIDELINER CATHETER, MODELS 5571, 5572, 5573
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 4, 2009 |
| Received | Jun 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091750
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.