# K101146: Water Bottle Cap System

- Pathway: 510(k) (Traditional)
- Applicant: United States Endoscopy Group, Inc.
- Decided: Jul 16, 2010 after 84 days
- Product code: FEQ (Pump, Air, Non-Manual, For Endoscope)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices 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.

## Most influential descendants
- K222734: Diversatek Healthcare PureFlo Irrigation System / Water Bottle Tubing (2022), 0 descendants of its own
- K112576: Endochoice Water Bottle Cap System (2012), 0 descendants of its own

## Indications for use
The Water Bottle Cap System is intended to be used with an air source from an endoscope with the purpose of supplying sterile water to the endoscope during endoscopic procedures. It is compatible with U.S. commercially available sterile water bottles.

Source page: https://510kreport.com/device/K101146
Methodology: https://510kreport.com/methodology