510(k) K001069

MODEL 4000 EEG MONITOR WITH PSI (PSA4000) by Physiometrix, Inc. — Product Code OLW

K001069 is an FDA 510(k) premarket notification submitted by Physiometrix, Inc. for the device "MODEL 4000 EEG MONITOR WITH PSI (PSA4000)". The FDA issued a decision of Substantially Equivalent on June 30, 2000. 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
June 30, 2000
Date Received
April 3, 2000
Clearance Type
Traditional
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.