# K905788: Model M1251A Mon. Full Disclosure Review System

- Pathway: 510(k) (Traditional)
- Applicant: Hewlett-Packard Co.
- Decided: Jun 6, 1991 after 161 days
- Product code: DXJ (Display, Cathode-Ray Tube, Medical)
- Device class: 2
- Regulation: 21 CFR 870.2450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 1 cites it directly.
0 of 13 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
- K962811: Spacelabs Medical Multi-Disclosure Workstation (1997), 11 descendants of its own
- K073372: Electrophysiology Systems Integrator (Epsi) (2007), 10 descendants of its own
- K083321: Cardio-View (2008), 9 descendants of its own
- K111320: Globalcardio (2011), 3 descendants of its own
- K122632: Guava II (2014), 2 descendants of its own

Source page: https://510kreport.com/device/K905788
Methodology: https://510kreport.com/methodology