FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STIMPOD NMS460 Nerve Stimulator
K Number: K252712
·
Decision May 28, 2026
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
1
Review Days
274
Basic Information
- Device Name
- STIMPOD NMS460 Nerve Stimulator
- K Number
- K252712
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5890
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Algiamed Technologies USA, Inc.
- Date Received
- August 27, 2025
- Decision Date
- May 28, 2026
- 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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