510(k) K895232 ยท LOS
MODEL ELI-100/ST ELECTROCARDIOGRAPH
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Dec 13, 1989 |
| Received | Aug 21, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895232
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.