# K001057: Agilent Information Center Software for M3150A and M3153A and Agilent M2/M3/M4 Compact Portable Patient Monitor

- Pathway: 510(k) (Special)
- Applicant: Agilent Technologies, Inc.
- Decided: May 3, 2000 after 30 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
470 later devices descend from it; 7 cite it directly.
0 of 471 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K013199: Philips Component Compact Monitor,Model M1275B, Philips Compenent Rack, Model M1276B (2001), 431 descendants of its own
- K021422: Philips Information Center Software Revision D.02 (2002), 426 descendants of its own
- K021300: Modification of Philips Component Compact Monitor, Release a.03, Model M1275B (2002), 421 descendants of its own
- K020531: Philips Multi-Parameter Module, Model M3001A; Philips Component Compact Monitor, Release a.02, Model M1275B (2002), 416 descendants of its own
- K021778: Philips Component Compact Monitor, Release a.04, Model #M1275B (2002), 407 descendants of its own

Source page: https://510kreport.com/device/K001057
Methodology: https://510kreport.com/methodology