510(k) K884504 ยท DPS Electrocardiograph
ELECTRODE GEL
| Applicant | Herbert Stanley Co., Skokie IL, US |
| Decision | Substantially Equivalent, Mar 9, 1989 |
| Received | Oct 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884504
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.