# K992328: Fuzzy Automatic Blood Pressure Monitor Models MD-750, MD-770, MD-800

- Pathway: 510(k) (Traditional)
- Applicant: Meditec Co., Ltd.
- Decided: Jul 21, 1999 after 9 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: 1 generation back to K952826 (1996). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K952826: Full Auto Fuzzy Blood Pressure Meter Model SE-7000, Sein Electronics Co., Ltd. (1996) Summary page 1.

## Most influential descendants
- K041491: Zewa MFM-007 Blood Pressure Monitor (2004), 0 descendants of its own
- K041789: Noninvasive Blood Pressure Monitor, Models MD-880B and MD-900T (2004), 0 descendants of its own

## Indications for use
Noninvasive measurement of systolic and diastolic' blood pressure and heart rate in adult patients, i.e., age 18 and above, in a home care environment.

Source page: https://510kreport.com/device/K992328
Methodology: https://510kreport.com/methodology