FDA 510(k)
FDA class 2
Substantially Equivalent
🇹🇼 Taiwan
TUNG FU AIRMATE TENS, VITALITY MODE, TF-DT001
K Number: K042107
·
Decision Mar 9, 2005
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
2
Review Days
217
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Basic Information
- Device Name
- TUNG FU AIRMATE TENS, VITALITY MODE, TF-DT001
- K Number
- K042107
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5890
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Tung FU Electric Co., Ltd.
- Date Received
- August 4, 2004
- Decision Date
- March 9, 2005
- Product Code
- GZJ
- 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 |
|---|---|---|---|
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | FDA class 2 | Neurology |
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Other Clearances by Tung FU Electric Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K061452 | TF-BP01 BLOOD PRESSURE MEASUREMENT SYSTEM | Jul 12, 2006 | Substantially Equivalent |