# K841788: Utah Disposable Pressure Transducer

- Pathway: 510(k) (Traditional)
- Applicant: Utah Medical Products, Inc.
- Decided: Mar 25, 1985 after 329 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.
7 later devices descend from it; 4 cite it directly.
0 of 8 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
- K070710: Accutrans Disposable Pressure Monitoring System (2007), 2 descendants of its own
- K991886: Pulsion Pulsiocath, Pulsion Pcco Monitoring Kit, Pulsion in-Line Injectate Sensor (2000), 1 descendant of its own
- K151040: Art-line Single channel blood pressure system, Art-line Double channel blood pressure system, Art-line Triple channel blood pressure system, IAP Monitoring Set with Disposable Transducer (2015), 0 descendants of its own
- K102033: Combitrans Monitoring Sets and Accessories (2011), 0 descendants of its own
- K101189: Reavillmed Pressure Monitoring System and Picc (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K841788
Methodology: https://510kreport.com/methodology