510(k) K001348 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
ST/AR ST AND ARRHYTHMIA SOFTWARE
| Applicant | Agilent Technologies, Inc., Andover MA, US |
| Decision | Substantially Equivalent, May 17, 2000 |
| Received | Apr 28, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001348
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.