510(k) K021912 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
M2376 DEVICELINK SYSTEM
| Applicant | Philips Medical Systems, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jun 24, 2002 |
| Received | Jun 11, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021912
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.