510(k) K961636
K961636 is an FDA 510(k) premarket notification submitted by Oxford Instruments, Plc. for the device "MEDILOG VISION". The FDA issued a decision of Substantially Equivalent on January 17, 1997. The device falls under product code OLZ (Automatic Event Detection Software For Polysomnograph With Electroencephalograph), a Class II device regulated under 21 CFR 882.1400. Oxford Instruments, Plc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 17, 1997
- Date Received
- April 29, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Automatic Event Detection Software For Polysomnograph With Electroencephalograph
- Device Class
- Class II
- Regulation Number
- 882.1400
- Review Panel
- NE
- Submission Type
Automatically mark electroencephalograph and polysomongraph signals in order to aid in identification of such events and annotation of prolonged PSG traces; Automatically calculate simple measures obtained from recorded signals (e.G. Magnitude, time, frequency and simple statistical measures of marked events); All output subject to verification by qualified user