FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Adhesive Electrodes
K Number: K160138
·
Decision Aug 11, 2016
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
2
Review Days
203
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Basic Information
- Device Name
- Adhesive Electrodes
- K Number
- K160138
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1320
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Gmdasz Manufacturing Co., Ltd.
- Date Received
- January 21, 2016
- Decision Date
- August 11, 2016
- 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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Other Clearances by Gmdasz Manufacturing Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K092546 | GMDASZ TENS ELECTRODES, MODELS CWN1005, DIA. 5CM, DWN2505, 5CMX5CM, CWN1007.DIA. 7CM, CWN2509,5CMX9CM | Dec 18, 2009 | Substantially Equivalent |