# K920894: Decompression Tubes

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Technologies
- Decided: Apr 28, 1992 after 67 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K161003: EndoVive One Step Button Low Profile Initial Placement PEG Kit with ENFit Connector, EndoVive Low Profile Button Replacement Gastrostomy Tube Kit with ENFit Connector, EndoVive Button Right Angle Feeding Set with ENFit Connector, EndoVive Button Bolus Feeding Set with ENFit Connector, EndoVive Button Decompression Tube with ENFit Connector (2016), 1 descendant of its own
- K191844: Fidmi Low Profile Enteral Feeding Device (2019), 0 descendants of its own
- K980145: Amt Decompression Tubes (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K920894
Methodology: https://510kreport.com/methodology