# K990127: Corflo Cubby Low Profile Gastrostomy Device (LPGD)

- Pathway: 510(k) (Special)
- Applicant: Corpak Medsystems
- Decided: Feb 10, 1999 after 28 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: none
- 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’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Corflo cuBBy LPGD is designed to allow for the administration of feeding solutions directly into the stomach of patients who are unable to take oral feedings but whose alimentary tracts are otherwise intact. It may also be used for gastric drainage with the aid of a decompression tube.

Source page: https://510kreport.com/device/K990127
Methodology: https://510kreport.com/methodology