510(k) K011093 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154
| Applicant | Agilent Technologies, Inc., Andover MA, US |
| Decision | Substantially Equivalent, May 1, 2001 |
| Received | Apr 10, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011093
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 28, 2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems Viridia/Agilent Information Center
Model :
M3150A#C01 Terminated |
None listed | |
| Feb 28, 2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems Viridia/Agilent Information Center
Model : M3151A#CO1 Terminated |
None listed | |
| Feb 28, 2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems Intellivue Information Center
Model: M3150B#C01 Terminated |
None listed | |
| Feb 28, 2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems Intellivue Information Center
Model: M3150BU#CO1 Terminated |
None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.