510(k) K001664 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
COMPACT PORTABLE PATIENT MONITOR WITH WIRELESS ALAN, MODEL ALILENT M3000A/M3046A OPTION J120
| Applicant | Agilent Technologies, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jun 30, 2000 |
| Received | May 31, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001664
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.