510(k) K070136 ยท DPS Electrocardiograph
AUDICOR 200 SYSTEM, MODELS 200D AND 200S
| Applicant | Inovise Medical, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Apr 13, 2007 |
| Received | Jan 16, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070136
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.