SEW
- Product code
- SEW
- Device name
- Automated Endoscope Channel Cleaner
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6994
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 2
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 2 (all years; only the last 3 years are listed here)
FDA classification definition
An automated endoscope channel cleaner is a device intended to replace all or a portion of manual cleaning of internal passages and ports of compatible reusable flexible endoscopes. Cleaning is conducted using an agent that exerts physical force (e.g., friction) on single or multiple channels of compatible endoscopes for removal of soil. This device type is not intended to provide or replace high-level disinfection or sterilization.
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K253267 | 2026-03-05 | Nanosonics Limited | CORIS System | |
| DEN240018 | 2025-03-19 | Nanosonics Limited | CORIS System | — |
Official FDA classification page: SEW
Classification and pathway per current FDA publications. Data from openFDA (CC0).