510(k) K070238 ยท DQY Catheter, Percutaneous
AMPLATZER RELIANT CATHETER DELIVERY SYSTEM
| Applicant | Aga Medical Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 28, 2007 |
| Received | Jan 25, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070238
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.