510(k) K964408 ยท DPS Electrocardiograph
POSEIDON CARDIAC MONITORING SYSTEM (PCMS)
| Applicant | Instromedix, Inc., Hillsboro OR, US |
| Decision | Substantially Equivalent, Jul 23, 1997 |
| Received | Nov 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964408
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.