510(k) K953663 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CORDIS WEBSTER T20 DIAGNOSTIC DEFLECTABLE TIP CATHETER
| Applicant | Cordis Webster, Inc., Baldwin Park CA, US |
| Decision | Substantially Equivalent, Sep 18, 1996 |
| Received | Aug 7, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953663
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.