510(k) K050558 ยท DTK Filter, Intravascular, Cardiovascular
MODIFICATION TO: RECOVERY FILTER SYSTEM, MODEL RF-210F
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Unknown, Aug 29, 2005 |
| Received | Mar 3, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050558
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.