510(k) K953175 ยท MLD Monitor, St Segment With Alarm
AS/3 ESTPR MODULE
| Applicant | Datex Division Instrumentarium Corp., Tewksbury MA, US |
| Decision | Substantially Equivalent, Feb 6, 1997 |
| Received | Jul 7, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953175
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.