510(k) K052083 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
NAVISTAR RMT STEERABLE TIP DIAGNOSTIC CATHETER
| Applicant | Biosense Webster, Inc., Diamond Bar CA, US |
| Decision | Substantially Equivalent, Sep 29, 2005 |
| Received | Aug 2, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052083
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.