510(k) K011824 ยท DSI Detector And Alarm, Arrhythmia
AGILENT M2636B TELEMON B MONITOR (TELEMON B)
| Applicant | Agilent Technologies, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jul 2, 2001 |
| Received | Jun 11, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011824
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.