X-trodes System M
by X-Trodes 510(k)
Active
510(k) K232210
Overview
The X-trodes System M is a physiological signal amplifier. It is designed to function as a medical device for the acquisition and processing of physiological signals.
This device has received FDA 510K clearance. It is categorized under neurology and operates according to regulation number 882.1835.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK232210 | Date4 Feb 2024 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 6 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- GWL
- Device Class
- Class II
- Regulation
- 21 CFR Part 882.1835
- Advisory Committee
- Neurology
- FDA Decision
- SESE Substantially Equivalent
Questions
What is the primary function of the X-trodes System M?
The X-trodes System M is a medical device specifically designed for the acquisition and processing of physiological signals. It is categorized within the field of neurology to assist in clinical signal monitoring.
Has the X-trodes System M received regulatory clearance?
Yes, the X-trodes System M has received FDA 510K clearance. This indicates that the device has been reviewed and found to be substantially equivalent to other legally marketed devices under regulation number 882.1835.
What medical specialty is this amplifier associated with?
The X-trodes System M is categorized under the neurology medical specialty. It operates according to the regulatory standards defined for physiological signal amplifiers used in neurological applications.