PHOENIX DIGITAL EEG SYSTEM— 510(k) K911229
Substantially EquivalentDantec Medical, Inc.
FDA 510(k) clearance K911229 for PHOENIX DIGITAL EEG SYSTEM, Substantially Equivalent on 1991-09-30. Applicant: Dantec Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Dantec Medical, 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
- Washington, DC, US
Recent devices under product code GWQ
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