510(k) K962307 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
RHYDER DIAGNOSTIC CATHETER
| Applicant | Fidus Medical Technology Corp., Fremont CA, US |
| Decision | Substantially Equivalent, Sep 17, 1996 |
| Received | Jun 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962307
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.