510(k) K091624 ยท DQY Catheter, Percutaneous
STENT GRAFT BALLOON CATHETER
| Applicant | Via Biomedical, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 15, 2009 |
| Received | Jun 3, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091624
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.