510(k) K020671
K020671 is an FDA 510(k) premarket notification submitted by Physiometrix, Inc. for the device "PSA4000 EEG MONITOR WITH FRONTAL PSI". The FDA issued a decision of Substantially Equivalent on October 4, 2002. The device falls under product code OLW (Index-Generating Electroencephalograph Software), a Class II device regulated under 21 CFR 882.1400. Physiometrix, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 4, 2002
- Date Received
- March 1, 2002
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Index-Generating Electroencephalograph Software
- Device Class
- Class II
- Regulation Number
- 882.1400
- Review Panel
- NE
- Submission Type
Analyze electrical activity of the brain by transformation of electroencephalograph signals into a dimensionless index number for use and interpretation by a qualified user.