510(k) K001436 ยท DSI Detector And Alarm, Arrhythmia
AGILENT M2636A TELEMON MONITOR
| Applicant | Agilent Technologies, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jun 7, 2000 |
| Received | May 8, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001436
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.