FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ELECTRODE, CUTANEOUS
K Number: K933801
·
Decision Oct 21, 1994
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
46
Review Days
443
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Basic Information
- Device Name
- ELECTRODE, CUTANEOUS
- K Number
- K933801
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1320
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Cadwell Laboratories, Inc.
- Date Received
- August 4, 1993
- Decision Date
- October 21, 1994
- 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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