FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MINGOGRAF EEG21
K Number: K802292
·
Decision Oct 3, 1980
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
66
Review Days
14
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Basic Information
- Device Name
- MINGOGRAF EEG21
- K Number
- K802292
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Siemens Corp.
- Date Received
- September 19, 1980
- Decision Date
- October 3, 1980
- Product Code
- GWQ
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GWQ | Full-Montage Standard Electroencephalograph | FDA class 2 | Neurology |
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