# K912188: Dinamap Plus Physiological Monitor Model 8700

- Pathway: 510(k) (Traditional)
- Applicant: Critikon Company, LLC
- Decided: Dec 4, 1991 after 201 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.
46 later devices descend from it; 2 cite it directly.
1 of 47 devices in its family (counting itself) has 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
- K955113: Dinamap Select Multi-Parameter System (1996), 44 descendants of its own
- K971569: Dinamap MPS Portable Monitor (1997), 43 descendants of its own
- K970182: Dinamap Compact Monitor (1997), 41 descendants of its own
- K992638: Dinamap Pro Series Monitor, Models 100, 200, 300, 400 (2000), 40 descendants of its own
- K014255: Dinamap Procare Series Monitor; Model 100, 200, 300, 400 (2002), 22 descendants of its own

Source page: https://510kreport.com/device/K912188
Methodology: https://510kreport.com/methodology