510(k) K902652 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MORTARA INSTRUMENT MODEL ELI 50
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Aug 23, 1990 |
| Received | Jun 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902652
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.