# K001100: Bioz.Com Hemodynamic Monitor with Bioz Tect Sensor and Bioz Tect Cable Impedance Plethysmograph

- Pathway: 510(k) (Special)
- Applicant: Cardiodynamics International Corp.
- Decided: May 5, 2000 after 30 days
- Product code: DSB (Plethysmograph, Impedance)
- Device class: 2
- Regulation: 21 CFR 870.2770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K011797: Bioztect Sensor and Bioztect Cable (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K001100
Methodology: https://510kreport.com/methodology