510(k) K932388 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
HRT SERIES 100 ELECTROPHYSIOLOGY CATHETER
| Applicant | Heart Rhythm Technologies, Inc., Temecula CA, US |
| Decision | Substantially Equivalent, May 31, 1995 |
| Received | May 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932388
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.