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BWIII EEG, BWIII EEG PLUS, BWIII PSG, BWIII PSG PLUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112107
510(k) Type
Traditional
Applicant
NEUROVIRTUAL USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2011
Days to Decision
98 days
Submission Type
Summary

BWIII EEG, BWIII EEG PLUS, BWIII PSG, BWIII PSG PLUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112107
510(k) Type
Traditional
Applicant
NEUROVIRTUAL USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2011
Days to Decision
98 days
Submission Type
Summary