# K072652: Enteral Feeding Spike Adapter

- Pathway: 510(k) (Traditional)
- Applicant: Cedic S.R.L.
- Decided: Jan 18, 2008 after 120 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.
10 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Zevex Spike Pump Set LGOO1O: named in the summary without a submission number

## Most influential descendants
- K140581: Cedic Enteral Distal End Enfit Transition Connector, Cedic Enteral Enfit Transition Connector for Medication Port (2014), 8 descendants of its own
- K150034: AMT Enteral Transition Adapters (2015), 1 descendant of its own
- K253268: Profoject Enteral/Oral Feeding Syringe; Profoject Reusable Enteral/Oral Feeding Syringe (Model A, Model B); Profoject ENFit Adaptor; Profoject Enteral Feeding Syringes Cap (2026), 0 descendants of its own
- K231299: Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector (2024), 0 descendants of its own
- K233190: ENFit Adaptor (2024), 0 descendants of its own

## Indications for use
For connecting a universal enteral spike set to a feeding container having a SpikeRight TM connection port.

Source page: https://510kreport.com/device/K072652
Methodology: https://510kreport.com/methodology