510(k) K983229
K983229 is an FDA 510(k) premarket notification submitted by Olympic Medical Corp. for the device "OLYMPIC MEDICAL LECTROMED CEREBRAL FUNCTION MONITOR SYSTEM". The FDA issued a decision of Substantially Equivalent on March 23, 1999. The device falls under product code OMA (Amplitude-Integrated Electroencephalograph), a Class II device regulated under 21 CFR 882.1400. Olympic Medical Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 23, 1999
- Date Received
- September 15, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Amplitude-Integrated Electroencephalograph
- Device Class
- Class II
- Regulation Number
- 882.1400
- Review Panel
- NE
- Submission Type
Measure and record electrical activity of the brain by acquisition of amplitude-integrated electroencephalograph (electroencephalograph signals that have been filtered and displayed in a specific manner).