# K853099: L.O.N. Pres Mon Lines, CPC Lines, Administration

- Pathway: 510(k) (Traditional)
- Applicant: L.O.N. Research, Inc.
- Decided: Dec 3, 1985 after 133 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K063851: Auto-Fill Syringe Kit, Model 7600 (2007), 1 descendant of its own
- K131661: Infusion Syringe Set (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K853099
Methodology: https://510kreport.com/methodology