510(k) K991531 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078
| Applicant | Cordis Webster, Inc., Baldwin Park CA, US |
| Decision | Substantially Equivalent, Oct 4, 1999 |
| Received | May 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991531
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.