# K944750: Corflo 300 Pump

- Pathway: 510(k) (Traditional)
- Applicant: Corpak, Inc.
- Decided: Jun 19, 1995 after 266 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: 1 (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
- Sep 19, 2011 · Not classified · Z-0089-2012: Corpak is removing the Corflo 300 Enteral Pump from the market due to the possibility that with fluid ingress or other damage, the keypad may not function, and the possibility of motor mount failure.

Source page: https://510kreport.com/device/K944750
Methodology: https://510kreport.com/methodology