510(k) K031182 ยท DPS Electrocardiograph
ELI 200+ AUDICOR
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jul 25, 2003 |
| Received | Apr 15, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031182
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.