510(k) K982835 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ELECTRODE SWITCHBOX, MODEL 11-081002
| Applicant | Cardima, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Oct 29, 1998 |
| Received | Aug 12, 1998 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K982835
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.