510(k) K955416 ยท DPS Electrocardiograph
CARDIMAX MODEL FX-2111
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Jul 15, 1996 |
| Received | Nov 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955416
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.