510(k) K023195 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MAGLIFE C/MAGLIFE C PLUS
| Applicant | Schiller Medical S.A., Wissembourg Cedex, FR |
| Decision | Substantially Equivalent, Jun 3, 2003 |
| Received | Sep 25, 2002 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K023195
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.