510(k) K993248 ยท MJN Catheter, Intravascular Occluding, Temporary
AMPLATZER SIZING BALLOON
| Applicant | Aga Medical Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 12, 2000 |
| Received | Sep 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993248
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.