FDA 510(k)
FDA class 2
Substantially Equivalent
🇪🇸 Spain
WiEMSpro
K Number: K181955
·
Decision Feb 12, 2019
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
2
Review Days
204
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Basic Information
- Device Name
- WiEMSpro
- K Number
- K181955
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5850
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medical Cables S.L.
- Date Received
- July 23, 2018
- Decision Date
- February 12, 2019
- Product Code
- NGX
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| NGX | Stimulator, Muscle, Powered, For Muscle Conditioning | FDA class 2 | Physical Medicine |
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Other Clearances by Medical Cables S.L.
| K Number | Device Name | ||
|---|---|---|---|
| K211298 | WiEMSpro | Aug 25, 2022 | Substantially Equivalent |