MODEL EEG-4217 ELECTROENCEPHALOGRAPH— 510(k) K791234
Substantially EquivalentNihon Kohden America, Inc.
FDA 510(k) clearance K791234 for MODEL EEG-4217 ELECTROENCEPHALOGRAPH, Substantially Equivalent on 1979-09-12. Applicant: Nihon Kohden America, Inc.. Device class: 2.
Clearance details
- Applicant
- Nihon Kohden America, Inc.
- Product code
- Code GWQ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Foothill, CA, US
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