# K050040: MS-753 Mars Inflate-Read Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Mars Medical Products
- Decided: Mar 30, 2005 after 82 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
L. The device is designed to provide signals from which systolic and diastolic pressures can be derived through the use of the Oscillometric method. The device also measure pulse rate, 2. The device is for adult use only. 3. The device is for use at home or while traveling.

Source page: https://510kreport.com/device/K050040
Methodology: https://510kreport.com/methodology