# K181982: MIDAScope and Introducer Kit, and MIDASystem

- Pathway: 510(k) (Traditional)
- Applicant: Intravu, Inc.
- Decided: Aug 21, 2018 after 27 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: 9 generations back to K833587 (1983). 42 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162475: mi-eye 2, mi-eye 2 monitor, Trice Medical (2016) Summary page 4.
- K141326: Needle View CH Scope Kits, Biovision Technologies, LLC (2014) Summary page 4.

## Most influential descendants
- K243020: MIDASVu (2024), 1 descendant of its own
- K252579: Orthoscan TAU MVP Mini C-Arm System (2026), 0 descendants of its own

## Indications for use
The MIDAScope™ and Introducer Kit, and MIDASystem™ are indicated for use in diagnostic and operative arthroscopic and endoscopic procedures to provide illumination and visualization of interior cavity joints and other body cavities through a natural or surgical opening.

Source page: https://510kreport.com/device/K181982
Methodology: https://510kreport.com/methodology