FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SKIN PURE
K Number: K862799
·
Decision Nov 13, 1986
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
68
Applicant Total
166
Review Days
114
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Basic Information
- Device Name
- SKIN PURE
- K Number
- K862799
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1275
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Nihon Kohden America, Inc.
- Date Received
- July 22, 1986
- Decision Date
- November 13, 1986
- Product Code
- GYB
- 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 |
|---|---|---|---|
| GYB | Media, Electroconductive | FDA class 2 | Neurology |
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