510(k) K052145

DATEX-OHMEDA S/5 BIS MODULE, E-BIS AND ACCESSORIES by GE Healthcare — Product Code OLW

K052145 is an FDA 510(k) premarket notification submitted by GE Healthcare for the device "DATEX-OHMEDA S/5 BIS MODULE, E-BIS AND ACCESSORIES". The FDA issued a decision of Substantially Equivalent on August 23, 2005. The device falls under product code OLW (Index-Generating Electroencephalograph Software), a Class II device regulated under 21 CFR 882.1400. GE Healthcare has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 23, 2005
Date Received
August 8, 2005
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.