510(k) K942379 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
DAIG DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Dec 27, 1994 |
| Received | May 9, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942379
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.