# K882682: Compat Enteral Delivery System

- Pathway: 510(k) (Traditional)
- Applicant: Sandoz Nutrition
- Decided: Oct 28, 1988 after 122 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.
17 later devices descend from it; 1 cites it directly.
0 of 18 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
- K073070: Dio Biotite-H Implant System (2008), 16 descendants of its own
- K112532: ET II Bio-SA Fixture System (2012), 10 descendants of its own
- K151626: ET III Bio-SA Fixture System (2016), 9 descendants of its own
- K203360: EK Implants and Abutments System (2022), 7 descendants of its own
- K221866: S-Plant Dental Implant System (2024), 2 descendants of its own

Source page: https://510kreport.com/device/K882682
Methodology: https://510kreport.com/methodology