510(k) K042998 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
REFSTAR RMT EXTERNAL REFERENCE PATCH
| Applicant | Biosense Webster, Inc., Diamond Bar CA, US |
| Decision | Substantially Equivalent, Sep 29, 2005 |
| Received | Nov 1, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K042998
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.