# K840932: Muse-DP

- Pathway: 510(k) (Traditional)
- Applicant: Marquette Electronics, Inc.
- Decided: Oct 30, 1984 after 242 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
78 later devices descend from it; 4 cite it directly.
0 of 79 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
- K980495: Muse Cardiovascular Information System (1998), 61 descendants of its own
- K992637: Muse Cardiovascular Information System (1999), 60 descendants of its own
- K023100: Accusketch Cardiac Quantitative System W/ Advanced Analysis Components (2002), 23 descendants of its own
- K042525: Centricity Radiology RA600/Centricity Cardiology CA1000/Centricity Digital Hardcopy Workstation (2004), 22 descendants of its own
- K050614: Muse Cardiology Information System (2005), 20 descendants of its own

Source page: https://510kreport.com/device/K840932
Methodology: https://510kreport.com/methodology