510(k) K981066 ยท LOS
FUKUDA DENSHI: CARDIOMAX, MODEL FX-4010 MULTI CHANNEL ELECTROCARDIOGRAPH
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Aug 31, 1998 |
| Received | Mar 24, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981066
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.