510(k) K091793 ยท DQY Catheter, Percutaneous
AMPLATZER TORQVUE 3 DELIVERY SHEATH, MODEL 9-TV3-08F104, 9-TV3-08F54
| Applicant | Aga Medical Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 9, 2009 |
| Received | Jun 17, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091793
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.