510(k) K860646 ยท DPS Electrocardiograph
PATIENT MON 1280/1281/120C/121C & MULTI-PARA CART
| Applicant | Analogic Corp., Peabody MA, US |
| Decision | Substantially Equivalent, Oct 16, 1986 |
| Received | Feb 20, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860646
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.