510(k) K033633 ยท DQY Catheter, Percutaneous
VASCON POLARIS GUIDING CATHETER
| Applicant | Vascon, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Feb 18, 2004 |
| Received | Nov 19, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033633
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.