FDA 510(k)
FDA class 2
Substantially Equivalent
🇹🇼 Taiwan
CONDUCTIVE GEL FOR ULTRASOUND
K Number: K002832
·
Decision Aug 6, 2001
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
68
Applicant Total
6
Review Days
329
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Basic Information
- Device Name
- CONDUCTIVE GEL FOR ULTRASOUND
- K Number
- K002832
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1275
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Skylark Device & Systems Co., Ltd.
- Date Received
- September 11, 2000
- Decision Date
- August 6, 2001
- 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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