510(k) K933404 ยท DPS Electrocardiograph
CRITIKON CENTRAL STATIN MONITOR
| Applicant | Critikon Company, LLC, Tampa FL, US |
| Decision | Substantially Equivalent, Feb 9, 1994 |
| Received | Jul 12, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933404
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.