# K945633: Neuro Channel Endoscope Model 2232

- Pathway: 510(k) (Traditional)
- Applicant: Clarus Medical Systems, Inc.
- Decided: Sep 19, 1995 after 307 days
- Product code: GWG (Endoscope, Neurological)
- Device class: 2
- Regulation: 21 CFR 882.1480
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K223615: Digital ClarusScope System, Digital NeuroPEN System (2023), 0 descendants of its own

## Recalls of this device
- Sep 15, 2003 · Not classified · Z-0049-04: Size mix-up. 13 cm product may be labeled as 21.6 mm and visaversa.

Source page: https://510kreport.com/device/K945633
Methodology: https://510kreport.com/methodology