# K990380: (1) Digital Blood Pressure Monitor, Model MD-250; (2) Fully Automatic Blood Pressure Monitor, Model MD-700

- Pathway: 510(k) (Traditional)
- Applicant: Meditec Co., Ltd.
- Decided: Feb 22, 1999 after 14 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 has not posted a summary or statement for it, so its predicates are not known.

Source page: https://510kreport.com/device/K990380
Methodology: https://510kreport.com/methodology