# K011824: Agilent M2636B Telemon B Monitor (Telemon B)

- Pathway: 510(k) (Special)
- Applicant: Agilent Technologies, Inc.
- Decided: Jul 2, 2001 after 21 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
Longest line of descent: 3 generations back to K894277 (1989). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001436: Agilent M2636A Telemon Monitor, Agilent Technologies, Inc. (2000) Summary page 3.
- K000854: Viridia Information Center Software for M3150A and M3153A, Viridia Telemetry System Transmitter, Agilent Technologies, Inc. (2000) Summary page 2.
- K993516: HP M2600A Viridia Telemetry System, Hewlett-Packard Co. (1999) Summary page 2.
- K991773: HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP Viridia Multi-Measurement Server and Compact Portable P, Hewlett-Packard GmbH (1999) Summary page 2.
- K981576: Multi-Parameter Module, Model M3000A & Display Unit, Model M3046A, Hewlett-Packard GmbH (1998) Summary page 3.
- K974567: Hewlett-Packard M2605A Viridia Wave Viewer, Hewlett-Packard Co. (1998) Summary page 3.
- K964122: HP Star ST and Arrhhythmia Software, Hewlett-Packard Co. (1997) Summary page 3.
- K941811: HP M1175A, M1176A, Component Monitoring System, Hewlett-Packard Co. (1994) Summary page 3.

## Indications for use
TeleMon is indicated for use in the monitoring, recording, and alarming of multiple physiologic parameters in adult and pediatric patients to gain information for treatment, to monitor adequacy of treatment, or to exclude causes of symptoms.

Source page: https://510kreport.com/device/K011824
Methodology: https://510kreport.com/methodology