510(k) K992373 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ORBITER ST DIAGNOSTIC ELECTRODE CATHETER & ORBITER ST EXTENSION CABLE
| Applicant | C.R. Bard, Inc., Lowell MA, US |
| Decision | Substantially Equivalent, Nov 5, 1999 |
| Received | Jul 15, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992373
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.