# K141119: Camera Enabled Probe

- Pathway: 510(k) (Traditional)
- Applicant: Trice Medical, Inc.
- Decided: Jul 29, 2014 after 90 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K833587 (1983). 24 ancestors in all.
7 later devices descend from it; 1 cites it directly.
0 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093717: C-Mor Visualization Device, Axis Surgical Technologies, Inc. (2010) Summary page 1.

## Most influential descendants
- K162475: mi-eye 2, mi-eye 2 monitor (2016), 6 descendants of its own
- K181982: MIDAScope and Introducer Kit, and MIDASystem (2018), 2 descendants of its own
- K243020: MIDASVu (2024), 1 descendant of its own
- K252579: Orthoscan TAU MVP Mini C-Arm System (2026), 0 descendants of its own
- K233115: Hawkeye Control Unit with Eyas Endoscope (2024), 0 descendants of its own

## Indications for use
The Camera Enabled Probe is indicated for use in diagnostic and operative arthroscopic and endoscopic procedures to provide illumination and visualization of an interior cavity of the body through either a natural or surgical opening.

Source page: https://510kreport.com/device/K141119
Methodology: https://510kreport.com/methodology