510(k) K133501 ยท DQY Catheter, Percutaneous
LEADLINER CS LEAD DELIVERY SYSTEM
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 25, 2014 |
| Received | Nov 14, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133501
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.