NICO BrainPath— 510(k) K172433
Substantially EquivalentNico Corporation
FDA 510(k) clearance K172433 for NICO BrainPath, Substantially Equivalent on 2017-09-07. Applicant: Nico Corporation. Device class: 2.
Clearance details
- Applicant
- Nico Corporation
- Product code
- Code GZT
- Device class
- Class 2
- Regulation
- 21 CFR 882.4800
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Indianapolis, IN, US
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More clearances from Nico Corporation
view allData sourced from openFDA. This site is unofficial and independent of the FDA.