Last synced on 27 January 2023 at 11:04 pm

DiscoverEEG System, Model DE-401

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142834
510(k) Type
Traditional
Applicant
NeuroWave Systems Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2015
Days to Decision
266 days
Submission Type
Summary

DiscoverEEG System, Model DE-401

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142834
510(k) Type
Traditional
Applicant
NeuroWave Systems Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/2015
Days to Decision
266 days
Submission Type
Summary