510(k) K884992 ยท DPS Electrocardiograph
FUKUDA DENSHI MODEL FX-1201
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Jan 12, 1989 |
| Received | Dec 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884992
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.