# K001670: Automatic Blood Pressure Monitor with Intellisense, Model Hem-757

- Pathway: 510(k) (Special)
- Applicant: Omron Healthcare, Inc.
- Decided: Jun 30, 2000 after 29 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.
127 later devices descend from it; 5 cite it directly.
0 of 128 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K030358: KD-622 Fully Automatic Electronic Blood Pressure Monitor (2003), 99 descendants of its own
- K070828: KD-595 Fully Automatic Electronic Blood Pressure Monitor (2007), 95 descendants of its own
- K080319: KD-591 Fully Automatic Electronic Blood Pressure Monitor (2008), 51 descendants of its own
- K090963: Fully Automatic Electronic Blood Pressure Monitor, Model KD-556 (2009), 46 descendants of its own
- K101950: Fully Automatic Electronic Blood Pressure Monitor Model KD-930 (2010), 34 descendants of its own

Source page: https://510kreport.com/device/K001670
Methodology: https://510kreport.com/methodology