510(k) K052362

BIS EEG MONITOR, MODEL A-3000 by Aspect Medical Systems, Inc. — Product Code OLW

K052362 is an FDA 510(k) premarket notification submitted by Aspect Medical Systems, Inc. for the device "BIS EEG MONITOR, MODEL A-3000". The FDA issued a decision of Substantially Equivalent on September 9, 2005. The device falls under product code OLW (Index-Generating Electroencephalograph Software), a Class II device regulated under 21 CFR 882.1400. Aspect Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 9, 2005
Date Received
August 29, 2005
Clearance Type
Special
Expedited Review
No
Third Party Review
Yes

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.