# K914838: Propaq 102,104,106,102EL,104EL,&106EL

- Pathway: 510(k) (Traditional)
- Applicant: Protocol Systems, Inc.
- Decided: Jan 10, 1992 after 77 days
- Product code: MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms))
- 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.
448 later devices descend from it; 3 cite it directly.
3 of 449 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K972020: Oscillomate Non-Invasive Blood Pressure Monitor (1998), 427 descendants of its own
- K980879: Oscillomate Nibp / SP02 Ems Monitor (1998), 426 descendants of its own
- K982776: 9303 Neonatal/Adult Vital Signs Monitor (1998), 425 descendants of its own
- K033048: Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS (2004), 272 descendants of its own
- K050844: 750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL, 750CM-2NL, 750C-3MS, 750CM-3MS, 750C-3NL, 750CM-3NL (2005), 264 descendants of its own

Source page: https://510kreport.com/device/K914838
Methodology: https://510kreport.com/methodology