510(k) K012094 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A
| Applicant | Agilent Technologies, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jul 20, 2001 |
| Received | Jul 5, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012094
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.