# K020341: Given Diagnostic System

- Pathway: 510(k) (Traditional)
- Applicant: Given Imaging, Ltd.
- Decided: May 2, 2002 after 90 days
- Product code: NEZ (System, Imaging, Gastrointestinal, Wireless, Capsule)
- Device class: 2
- Regulation: 21 CFR 876.1300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to DEN010002 (2001). 1 ancestor in all.
39 later devices descend from it; 12 cite it directly.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- DEN010002: Given Diagnostic Imaging System, Given Imaging, Ltd. (2001). Our OCR of the scanned summary read K010312, which is not in FDA’s 510(k) list. The device the summary names is FDA’s De Novo DEN010002, Given Diagnostic Imaging System (Given Imaging, Ltd.), granted Aug 1, 2001; older De Novo requests were first filed under a 510(k) number, so this links to the grant.

## Most influential descendants
- K022362: Given Diagnostics System (2002), 38 descendants of its own
- K022980: Modification to Given Diagnostic System (2003), 37 descendants of its own
- K031033: Given Diagnostic System (2003), 36 descendants of its own
- K032405: Given Diagnostic System (2003), 35 descendants of its own
- K040248: Modification to Given Diagnostic System (2004), 34 descendants of its own

## Indications for use
The Given® Diagnostic System is intended for visualization of the small bowel mucosa. It may be used as an adjunctive tool in the detection of abnormalities of the small bowel

Source page: https://510kreport.com/device/K020341
Methodology: https://510kreport.com/methodology