The following data is part of a premarket notification filed by Brain Sentinel, Inc. with the FDA for Speac System.
Device ID | K182180 |
510k Number | K182180 |
Device Name: | SPEAC System |
Classification | Physiological Signal Based Seizure Monitoring System |
Applicant | Brain Sentinel, Inc. 8023 Vantage Dr., Suite 216 San Antonio, TX 78230 |
Contact | Richard Waite |
Correspondent | Richard Waite Brain Sentinel, Inc. 8023 Vantage Dr., Suite 216 San Antonio, TX 78230 |
Product Code | POS |
CFR Regulation Number | 882.1580 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-13 |
Decision Date | 2019-05-11 |