510(k) K182180
K182180 is an FDA 510(k) premarket notification submitted by Brain Sentinel, Inc. for the device "SPEAC System". The FDA issued a decision of Substantially Equivalent on May 11, 2019. The device falls under product code POS (Physiological Signal Based Seizure Monitoring System), a Class II device regulated under 21 CFR 882.1580. Brain Sentinel, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 11, 2019
- Date Received
- August 13, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Physiological Signal Based Seizure Monitoring System
- Device Class
- Class II
- Regulation Number
- 882.1580
- Review Panel
- NE
- Submission Type
The Physiological signal based seizure monitoring system is a prescription device that uses physiological signal to identify abnormal physiological activity that may be associated with a seizure. The System does not predict seizure onsets, and is not intended as a standalone seizure monitoring device.