510(k) K001057 ยท DSI Detector And Alarm, Arrhythmia
AGILENT INFORMATION CENTER SOFTWARE FOR M3150A AND M3153A AND AGILENT M2/M3/M4 COMPACT PORTABLE PATIENT MONITOR
| Applicant | Agilent Technologies, Inc., Andover MA, US |
| Decision | Substantially Equivalent, May 3, 2000 |
| Received | Apr 3, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001057
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.