# K082564: Hyperq System

- Pathway: 510(k) (Special)
- Applicant: Biological Signal Processing, Ltd.
- Decided: Oct 20, 2008 after 46 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K102579: Hyperq AD-100 System (2010), 1 descendant of its own
- K140020: Hyperq Acs-100 System (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K082564
Methodology: https://510kreport.com/methodology