510(k) K800004 ยท DPS Electrocardiograph
ECG MONITOR OSCILLOSCOPE MODEL OEC-3200
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Mar 5, 1980 |
| Received | Jan 2, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800004
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.