510(k) K041772 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DATEX-OHMEDA PRESTN.01 MODULE (MODEL FAMILY M-PRESTN.01) AND ACCESSORIES
| Applicant | Datex-Ohmeda, Needham MA, US |
| Decision | Substantially Equivalent, Jul 28, 2004 |
| Received | Jul 1, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041772
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.