510(k) K113658 ยท KRD Device, Vascular, For Promoting Embolization
AMPLATZER VASCULAR PLUG 4
| Applicant | Aga Medical Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 12, 2012 |
| Received | Dec 12, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113658
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.