NXPRO Neuromuscular Electrical Stimulation Device— 510(k) K191181
Substantially EquivalentNeux Technologies, Inc.
FDA 510(k) clearance K191181 for NXPRO Neuromuscular Electrical Stimulation Device, Substantially Equivalent on 2019-10-11. Applicant: Neux Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Neux Technologies, Inc.
- Product code
- Code NGX
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tampa, FL, US
Recent devices under product code NGX
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