# K021240: Eikon Automatic Digital Blood Pressure Monitor, Model HD-200M/HD-200

- Pathway: 510(k) (Traditional)
- Applicant: Eikon Healthcare Device Corp.
- Decided: Nov 8, 2002 after 204 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The EIKON automatic digital blood pressure monitor, Model HD-200M / HD-200, is a noninvasive blood pressure measurement system intended to measure the systolic and diastolic blood pressures and pulse rate of an adult individual, over age 16, at home by using a non-invasive technique in which an inflatable cuff is wrapped around the arm. The cuff circumference is limited to be 7”- 15”.

Source page: https://510kreport.com/device/K021240
Methodology: https://510kreport.com/methodology