510(k) K050472 ยท DRA Catheter, Steerable
LYSUS INFUSION SYSTEM
| Applicant | Ekos Corp., Bothell WA, US |
| Decision | Substantially Equivalent, Mar 11, 2005 |
| Received | Feb 24, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050472
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.