510(k) K051217 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DATEX-OHMEDA PRESTIN MODULE (MODEL FAMILY E-PRESTIN, INCLUDING E-PRESTIN, E-RESTIN, E=PRETIN, E-PP AND E-PT/E-P)
| Applicant | GE Healthcare, Needham MA, US |
| Decision | Substantially Equivalent, Feb 3, 2006 |
| Received | May 12, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051217
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.