510(k) K041401 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MODIFICATION TO M2376A DEVICELINK SYSTEM
| Applicant | Philips Medical Systems, Boblingen, DE |
| Decision | Substantially Equivalent, Jun 4, 2004 |
| Received | May 26, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041401
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.