MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM— 510(k) K891383
Substantially EquivalentOxford Medilog, Inc.
FDA 510(k) clearance K891383 for MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM, Substantially Equivalent on 1989-06-01. Applicant: Oxford Medilog, Inc.. Device class: 2.
Clearance details
- Applicant
- Oxford Medilog, Inc.
- Product code
- Code OLZ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Clearwater, FL, US
Recent devices under product code OLZ
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