# K930459: Bard Mini-Infuser 1500 & 3000

- Pathway: 510(k) (Traditional)
- Applicant: Bard Medsystems Div.
- Decided: Aug 10, 1993 after 194 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Mar 4, 2011 · Class III · Z-2269-2012: Should a battery with the minimum contact diameter (.51 inches) be placed on the battery spring (.53 inches), an electrical circuit will not be completed and the Mini-Infuser will not operate. The rea
- Mar 4, 2011 · Class III · Z-2268-2012: Should a battery with the minimum contact diameter (.51 inches) be placed on the battery spring (.53 inches), an electrical circuit will not be completed and the Mini-Infuser will not operate. The rea

Source page: https://510kreport.com/device/K930459
Methodology: https://510kreport.com/methodology