FDA 510(k)
FDA class 2
Substantially Equivalent
🇳🇱 Netherlands
FLEXIBLE RUBBER ELECTRODES, MODELS: 1460265, 1460272, 1460274, 3444128, 3444129, 3444130
K Number: K030297
·
Decision Apr 28, 2003
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
5
Review Days
90
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Basic Information
- Device Name
- FLEXIBLE RUBBER ELECTRODES, MODELS: 1460265, 1460272, 1460274, 3444128, 3444129, 3444130
- K Number
- K030297
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1320
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Enraf-Nonius, B.V.
- Date Received
- January 28, 2003
- Decision Date
- April 28, 2003
- Product Code
- GXY
- 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 |
|---|---|---|---|
| GXY | Electrode, Cutaneous | FDA class 2 | Neurology |
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