510(k) K031781 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DATEX-OHMEDA PRESTN MODULE, (MODEL FAMILY M-PRESTN) AND ACCESSORIES
| Applicant | Datex-Ohmeda, Needham MA, US |
| Decision | Substantially Equivalent, Jun 25, 2003 |
| Received | Jun 10, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031781
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.