FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Transcutaneous Electrical Nerve Stimulator (RJTENS-2)
K Number: K252688
·
Decision Nov 24, 2025
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
227
Applicant Total
4
Review Days
90
Basic Information
- Device Name
- Transcutaneous Electrical Nerve Stimulator (RJTENS-2)
- K Number
- K252688
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5890
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bozhou Rongjian Medical Appliance Co., Ltd.
- Date Received
- August 26, 2025
- Decision Date
- November 24, 2025
- Product Code
- NUH
- 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 |
|---|---|---|---|
| NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter | FDA class 2 | Neurology |
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