FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CADWELL SPIKE AND SEIZURE DETECTOR
K Number: K140552
·
Decision Jul 23, 2014
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
40
Applicant Total
2
Review Days
141
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Basic Information
- Device Name
- CADWELL SPIKE AND SEIZURE DETECTOR
- K Number
- K140552
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1400
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Cadwell
- Date Received
- March 4, 2014
- Decision Date
- July 23, 2014
- Product Code
- OMB
- 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 |
|---|---|---|---|
| OMB | Automatic Event Detection Software For Full-Montage Electroencephalograph | FDA class 2 | Neurology |
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Other Clearances by Cadwell
| K Number | Device Name | ||
|---|---|---|---|
| K123589 | CADWELL DISPOSABLE PROBE HANDLE | Mar 19, 2013 | Substantially Equivalent |