510(k) K861850 ยท DPS Electrocardiograph
BURDICK DIVISION (E-500)
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Aug 28, 1986 |
| Received | May 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861850
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.