# K140315: US Endoscopy Distal Attachment Cap

- Pathway: 510(k) (Traditional)
- Applicant: United States Endoscopy Group, Inc.
- Decided: Apr 4, 2014 after 53 days
- Product code: OCX (Endoscopic Irrigation/Suction System)
- 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.
3 later devices descend from it; 1 cites 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K202616: ClearCap Distal Attachment (2021), 2 descendants of its own
- K260423: Disposable Endoscopic Distal Attachments (2026), 0 descendants of its own
- K242134: ClearCap Distal Attachment (2024), 0 descendants of its own

## Indications for use
The US Endoscopy Distal Attachment Cap has been designed to be attached to the distal end of the endoscope to facilitate endoscopic therapy. The US Endoscopy Distal Attachment Cap is intended for the following. • Gastrointestinal mucosal resection (endoscopic mucosal resection) • Keeping the suitable depth of the endoscope's view field

Source page: https://510kreport.com/device/K140315
Methodology: https://510kreport.com/methodology