510(k) K894500 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
DAIG ELECTROPHYSIOLOGY CATHETER
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Sep 18, 1989 |
| Received | Jul 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894500
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 6, 2014 | St Jude Medical St. Jude Medical, Fixed Curve Response 6F Electrophysiology Catheter, CSL, Model 401353 Terminated |
DRF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.