# K001433: CNS-9300 Series Central Station

- Pathway: 510(k) (Traditional)
- Applicant: Nihon Kohden America, Inc.
- Decided: Nov 7, 2000 after 183 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K023475: CNS-9700 Series Central Nurse Station and Accessories (2002), 3 descendants of its own
- K073550: Prefense Edns-9000 Series Nurse Central Station (2008), 1 descendant of its own
- K102106: Nihon Khden Prefense Edns-9000 Series Central Nurse Station (2010), 0 descendants of its own
- K102376: Nihon Kohden CNS-6200 Series Central Nurse Station, Model CNS-6201 (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K001433
Methodology: https://510kreport.com/methodology