# K801008: Multi-AD Fluid Dispensing Pump MP-3000

- Pathway: 510(k) (Traditional)
- Applicant: Burron Medical Products, Inc.
- Decided: Jun 2, 1980 after 35 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.
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
- K980109: Cyclotech Cyclosporine Oral Solutions Dispenser (1998), 1 descendant of its own
- K143177: KleenGel Dispenser (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K801008
Methodology: https://510kreport.com/methodology