510(k) K020671

PSA4000 EEG MONITOR WITH FRONTAL PSI by Physiometrix, Inc. — Product Code OLW

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.