510(k) K042110 ยท EZL Catheter, Retention Type, Balloon
BEAMCATH
| Applicant | Beampoint AB, Minneapolis, MN, US |
| Decision | Substantially Equivalent, Feb 25, 2005 |
| Received | Aug 5, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042110
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.