FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇱 Israel
NEURITOR 2001
K Number: K902752
·
Decision Dec 4, 1990
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
186
Applicant Total
1
Review Days
165
Basic Information
- Device Name
- NEURITOR 2001
- K Number
- K902752
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- IMEXCO GENERAL LTD.
- Date Received
- June 22, 1990
- Decision Date
- December 4, 1990
- 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 |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GWQ), ordered by most recent decision date.
Flexset System
FDA 510(k)
FDA Class 2
·Neurology
Neuronaute Plus
FDA 510(k)
FDA Class 2
·Neurology
Q21
FDA 510(k)
FDA Class 2
·Neurology
SPARK Scan
FDA 510(k)
FDA Class 2
·Neurology
Cumulus Functional Neurophysiology Platform
FDA 510(k)
FDA Class 2
·Neurology
Okti
FDA 510(k)
FDA Class 2
·Neurology