# K063137: Pharmasmart Public Use Blood Pressure Monitor, Models PS-1000/PS-1500/PS-2000

- Pathway: 510(k) (Traditional)
- Applicant: Pharmasmart, Inc.
- Decided: May 1, 2007 after 197 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
Longest line of descent: 4 generations back to K910772 (1991). 11 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040562: Lifeclinic, Model 2400, Lifeclinic International, Inc. (2004) Summary page 1.
- K982776: 9303 Neonatal/Adult Vital Signs Monitor, Cas Medical Systems, Inc. (1998) Summary page 1.

## Most influential descendants
- 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
- K153600: Consult Station TS (2017), 0 descendants of its own
- K140360: Health Kiosk (2015), 0 descendants of its own
- K113402: Solohealth Station (2012), 0 descendants of its own

## Indications for use
The PharmaSmart Models PS-1000, PS-1500 and PS-2000 are indicated for use for non-invasive oscillometric blood pressure and pulse rate monitoring by the general public in a sit down kiosk form. The device does not perform any diagnoses; it only provides pressure and rate data to the users, who are advised to consult a physician.

Source page: https://510kreport.com/device/K063137
Methodology: https://510kreport.com/methodology