510(k) K093476 ยท DQY Catheter, Percutaneous
AMPLATZER TORQ VUE 2 DELIVERY SHEATH MODEL 9-TV2-05F120, MODEL 9-TV2-06F120, MODELTV-2-07F120
| Applicant | Aga Medical Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 5, 2010 |
| Received | Nov 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093476
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.