# K951129: Novatrans II

- Pathway: 510(k) (Traditional)
- Applicant: Medex, Inc.
- Decided: Apr 5, 1995 after 23 days
- Product code: DRS (Transducer, Blood-Pressure, Extravascular)
- Device class: 2
- Regulation: 21 CFR 870.2850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K961404: MX960 Reusable Pressure Transducer (1996), 2 descendants of its own
- K221782: Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes (2023), 0 descendants of its own
- K981745: Biotrans Reusable Sensor Base Model Number BT Xxxxxx (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K951129
Methodology: https://510kreport.com/methodology