# K941188: Clarus Neuro Endoscope  (Model 2230)

- Pathway: 510(k) (Traditional)
- Applicant: Clarus Medical Systems, Inc.
- Decided: Apr 25, 1995 after 407 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
No predicates in its family tree.
2 later devices descend from it; 1 cites 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K974579: Percscope Model 2600 (1998), 1 descendant of its own
- K240535: Digital ClarusScope System; Digital NeuroPEN System (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K941188
Methodology: https://510kreport.com/methodology