510(k) K911140 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
BARD(R) ENDOCARDIAL BALLOON ARRAY
| Applicant | C.R. Bard, Inc., Tewksbury MA, US |
| Decision | Substantially Equivalent, May 7, 1991 |
| Received | Mar 14, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911140
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.