510(k) K933156 ยท DPS Electrocardiograph
DATEX AS/3 PATIENT MONITOR
| Applicant | Datex Division Instrumentarium Corp., Helsinki, FI |
| Decision | Substantially Equivalent, Dec 30, 1994 |
| Received | Jun 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933156
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.