510(k) K090120 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
REFSTAR PLUS WITH QWIKPATCH EXTERNAL REFERENCE PATCH, MODEL D-1210-03, REFSTAR PLUS CABLE, MODEL M-4700-106
| Applicant | Biosense Webster, Inc., Diamond Bar CA, US |
| Decision | Substantially Equivalent, Mar 24, 2009 |
| Received | Jan 21, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090120
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.