510(k) K960542 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
NOGA
| Applicant | Biosense, Ltd., Tirat Hacarmel, Haifa, IL |
| Decision | Substantially Equivalent, Apr 15, 1996 |
| Received | Feb 7, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960542
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.