FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODEL EEG 4400 WITH OPTIONAL ACCESSORIES
K Number: K874796
·
Decision Jan 19, 1988
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
186
Applicant Total
166
Review Days
75
Basic Information
- Device Name
- MODEL EEG 4400 WITH OPTIONAL ACCESSORIES
- K Number
- K874796
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- NIHON KOHDEN AMERICA, INC.
- Date Received
- November 5, 1987
- Decision Date
- January 19, 1988
- 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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