510(k) K992965 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085
| Applicant | Cordis Webster, Inc., Baldwin Park CA, US |
| Decision | Substantially Equivalent, Nov 26, 1999 |
| Received | Sep 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992965
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.