510(k) K834602 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
SWITCHING UNIT ELECTRODE CATHETER
| Applicant | Webster Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 9, 1984 |
| Received | Dec 30, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834602
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.