510(k) K052145
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.