510(k) K961247 ยท DPS Electrocardiograph
AS/3 LIGHT MONITOR
| Applicant | Datex Division Instrumentarium Corp., Tewksbury MA, US |
| Decision | Substantially Equivalent, Oct 23, 1996 |
| Received | Apr 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961247
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.