DYNAMIC NEUROSCREENING DEVICE— 510(k) K141208
Substantially EquivalentProsenex
FDA 510(k) clearance K141208 for DYNAMIC NEUROSCREENING DEVICE, Substantially Equivalent on 2014-07-23. Applicant: Prosenex. Device class: 1.
Clearance details
- Applicant
- Prosenex
- Product code
- Code LQW
- Device class
- Class 1
- Regulation
- 21 CFR 882.1200
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Leola, PA, US
Recent devices under product code LQW
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