510(k) K091370 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
RADIA STEERABLE DIAGNOSTIC CATHETER
| Applicant | C.R. Bard, Inc., Lowell MA, US |
| Decision | Substantially Equivalent, Jun 5, 2009 |
| Received | May 8, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091370
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.