# K792227: Multi-AD Fluid Dispensing System

- Pathway: 510(k) (Traditional)
- Applicant: National Patent Development Corp.
- Decided: Dec 20, 1979 after 45 days
- Product code: KYX (Dispenser, Liquid Medication)
- Device class: 1
- Regulation: 21 CFR 880.6430
- 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; 3 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
- K063851: Auto-Fill Syringe Kit, Model 7600 (2007), 1 descendant of its own
- K131661: Infusion Syringe Set (2013), 0 descendants of its own
- K955398: Formulation Preparation Device (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K792227
Methodology: https://510kreport.com/methodology