510(k) K881966 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ELECTROPHYSIOLOGY ELECTRODE CATH. W/SILVER/SILVER
| Applicant | C.R. Bard, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, Oct 4, 1988 |
| Received | May 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881966
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.