# K942700: Dinamap Vital Signs Monitor Models 9300 and 9320/9340

- Pathway: 510(k) (Traditional)
- Applicant: Critikon Company, LLC
- Decided: Mar 1, 1995 after 266 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.
42 later devices descend from it; 1 cites it directly.
1 of 43 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
- 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
- K022193: Dinamap Procare Series Monitor, Models 100N, 200N, 300N, 400N (2002), 21 descendants of its own
- K073203: Carescape V100 (2007), 20 descendants of its own

Source page: https://510kreport.com/device/K942700
Methodology: https://510kreport.com/methodology