# K983616: Daiwa Model 180

- Pathway: 510(k) (Traditional)
- Applicant: Daiwa Products, Inc.
- Decided: Oct 15, 1999 after 366 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 Daiwa Model 180 Automatic Inflation Wrist Digital Blood Pressure Monitor is designed to provide signals from which systolic and diastolic pressures can be derived through the use of the oscillometric method. The device also measures the heart rate. The device is for adult use only and measures wrist circumferences from 5 1/4” to 7 3/4”. The end user should not have common arrhythmias, such as atrial or ventricular premature beats or atrial fibrillation

Source page: https://510kreport.com/device/K983616
Methodology: https://510kreport.com/methodology