510(k) K802368 ยท DPS Electrocardiograph
OPTION 301 PACEMAKER EVAL. MODULE MAC-1
| Applicant | Marquette Electronics, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 4, 1981 |
| Received | Sep 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802368
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.