# K850893: BP/Clinic Sys Measurement, BP Non-Invasive

- Pathway: 510(k) (Traditional)
- Applicant: Sun Dance Technology, Inc.
- Decided: May 16, 1985 after 73 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 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
- K040562: Lifeclinic, Model 2400 (2004), 8 descendants of its own
- K063137: Pharmasmart Public Use Blood Pressure Monitor, Models PS-1000/PS-1500/PS-2000 (2007), 5 descendants of its own
- K063008: Health Check Kiosk (2007), 4 descendants of its own
- K093389: Csi Model 5K Managed Health System Kiosk (2009), 3 descendants of its own
- K101198: Csi Managed Health System Model: Csi Model 9K (2010), 1 descendant of its own

Source page: https://510kreport.com/device/K850893
Methodology: https://510kreport.com/methodology