510(k) K001621 ยท MJN Catheter, Intravascular Occluding, Temporary
DARDIK CAROTID SHUNT
| Applicant | Vascutech, Inc., Burlington MA, US |
| Decision | Substantially Equivalent, Dec 6, 2000 |
| Received | May 26, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001621
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.