# K911884: Advance Pressure Monitor/High Pressure Lines

- Pathway: 510(k) (Traditional)
- Applicant: Advance Medical Designs, Inc.
- Decided: Jul 5, 1994 after 1,163 days
- Product code: DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 2 cite it directly.
0 of 9 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
- K963749: High Pressure Injection Lines (1996), 7 descendants of its own
- K023591: Ultra High Pressure Injector Lines (2003), 3 descendants of its own
- K071196: Disposable High Pressure Injection Lines with and Without Rotating Adapters (2007), 2 descendants of its own
- K152387: Fluent Inflation Device (2015), 1 descendant of its own
- K162272: Fluent inflation device (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K911884
Methodology: https://510kreport.com/methodology