510(k) K093177 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
INTELLIBRIDGE SYSTEM
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Dec 18, 2009 |
| Received | Oct 8, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093177
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.