510(k) K980961 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.
| Applicant | Cordis Webster, Inc., Baldwin Park CA, US |
| Decision | Substantially Equivalent, May 28, 1998 |
| Received | Mar 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980961
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.