510(k) K071699 ยท KRD Device, Vascular, For Promoting Embolization
AMPLATZER VASCULAR PLUG II, MODELS AVP2-003, AVP2-018, AVP2-020, AVP2-022
| Applicant | Aga Medical Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Aug 15, 2007 |
| Received | Jun 21, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071699
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.