510(k) K112100 ยท DQY Catheter, Percutaneous
M2 NAVIGATION CATHETER AND GUIDELINER NAVIGATION CATHETER
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 20, 2012 |
| Received | Jul 22, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112100
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.