# K980429: HP M2600A Viridia Telemetry System (Formerly Known as the HP 2600A Omni-Care Telemetry System)

- Pathway: 510(k) (Traditional)
- Applicant: Hewlett-Packard Co.
- Decided: Sep 9, 1998 after 217 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: 1 generation back to K894277 (1989). 4 ancestors in all.
337 later devices descend from it; 2 cite it directly.
0 of 342 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K894277: M1400A Transmitter,M1402 Receiver,M1401 Mainframe, Hewlett-Packard Co. (1989) Summary page 1.
- K911139: Hewlett-Packard Models M1400A, M1402A & M1401A, Hewlett-Packard Co. (1991) Summary page 1.
- K913533: Model M1403A Telemetry Monitoring Systems (TMS), Hewlett-Packard Co. (1991) Summary page 1.
- K920429: Modified Model M1403A Telemetry Monitoring System, Hewlett-Packard Co. (1993) Summary page 1.

## Most influential descendants
- K993516: HP M2600A Viridia Telemetry System (1999), 336 descendants of its own
- K040357: M3290A Intellivue Information Center Software Release F.O and the M4840A Telemetry Monitoring System II (2004), 260 descendants of its own
- K041235: Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient Monitors (2004), 252 descendants of its own
- K042845: The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient Monitors (2004), 251 descendants of its own
- K050141: The Philips MP20, MP30, MP40, MP50, MP60, MP70 and MP90 Intellivue Patient Monitors (2005), 250 descendants of its own

## Indications for use
The indications for use of the Viridia Telemetry System are: « Condition: the licensed clinician decides that the Viridia Telemetry System should be used to monitor the patient. » Prescription versus over-the-counter: Viridia Telemetry System is a prescription device. « Part of body or type of tissue interacted with: The ECG signal is obtained from accessory electrodes in contact with the patient’s skin. The SpO; signal is obtained from an accessory sensor in contact with the patient’s skin. « Frequency of use: As prescribed by licensed clinician. « Physiological purpose: To monitor the ECG or Sp0O; of patients on the order of a licensed clinician. « Patient population: Adult and pediatric patients.

Source page: https://510kreport.com/device/K980429
Methodology: https://510kreport.com/methodology