# K842352: Pressure Monitoring Kit

- Pathway: 510(k) (Traditional)
- Applicant: Utah Medical Products, Inc.
- Decided: Mar 25, 1985 after 283 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K991886: Pulsion Pulsiocath, Pulsion Pcco Monitoring Kit, Pulsion in-Line Injectate Sensor (2000), 1 descendant of its own
- K101189: Reavillmed Pressure Monitoring System and Picc (2010), 0 descendants of its own
- K020587: Pulsion Pulsiocath Picco Monitoring Kit, Injectate Sensor Temperature Housing PV 4046 (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K842352
Methodology: https://510kreport.com/methodology