Neuvotion NeuStim NN-01— 510(k) K240632
Substantially EquivalentNeuvotion, Inc.
FDA 510(k) clearance K240632 for Neuvotion NeuStim NN-01, Substantially Equivalent on 2024-11-22. Applicant: Neuvotion, Inc.. Device class: 2.
Clearance details
- Applicant
- Neuvotion, Inc.
- Product code
- Code GZI
- Device class
- Class 2
- Regulation
- 21 CFR 882.5810
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
Recent devices under product code GZI
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