NEUCODIA— 510(k) K081591
Substantially EquivalentVerisci Corporation
FDA 510(k) clearance K081591 for NEUCODIA, Substantially Equivalent on 2009-05-15. Applicant: Verisci Corporation. Device class: 2.
Clearance details
- Applicant
- Verisci Corporation
- Product code
- Code GWE
- Device class
- Class 2
- Regulation
- 21 CFR 882.1890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raritan, NJ, US
Recent devices under product code GWE
view allData sourced from openFDA. This site is unofficial and independent of the FDA.