510(k) K983653 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
RADII DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER, MODEL # 30411 B, C AND D
| Applicant | Cardiac Pathways Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Dec 22, 1998 |
| Received | Oct 19, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983653
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.