FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NUAMPS
K Number: K023536
·
Decision Jan 15, 2003
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
53
Applicant Total
3
Review Days
86
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Basic Information
- Device Name
- NUAMPS
- K Number
- K023536
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Neuroscan
- Date Received
- October 21, 2002
- Decision Date
- January 15, 2003
- Product Code
- OLT
- 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 |
|---|---|---|---|
| OLT | Non-Normalizing Quantitative Electroencephalograph Software | FDA class 2 | Neurology |
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